Clinical Research Trials Archive – Closed Trials

This is our archive of closed clinical trials, which means that they are no longer accepting new participants or have been concluded. Once a research facility has chosen to close the study, it is sorted into the GPS archive by indication. If you are interested in enrolling in a clinical trial, then please browse our list of active clinical studies.

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We've found
15,024
archived clinical trials in
Infectious Disease

A Bioequivalence Study of Two Ciprofloxacin/Dexamethasone Formulations in Patients With Otitis Externa
A Randomized, Double-Blind, Placebo-Controlled, Parallel Design, Multiple-Site Study to Evaluate the Clinical Equivalence of Ciprofloxacin 0.3%/Dexamethasone 0.1% Sterile Otic Suspension (Par) Compared to CIPRODEX® (Ciprofloxacin 0.3%/Dexamethasone 0.1%) Sterile Otic Suspension (Alcon) in the Treatment of Adults With Acute Bacterial Otitis Externa
Status: Enrolling
Updated:  7/25/2013
Medical Consulting Center
2731
mi
from 98109
Miami, FL
A Bioequivalence Study of Two Ciprofloxacin/Dexamethasone Formulations in Patients With Otitis Externa
A Randomized, Double-Blind, Placebo-Controlled, Parallel Design, Multiple-Site Study to Evaluate the Clinical Equivalence of Ciprofloxacin 0.3%/Dexamethasone 0.1% Sterile Otic Suspension (Par) Compared to CIPRODEX® (Ciprofloxacin 0.3%/Dexamethasone 0.1%) Sterile Otic Suspension (Alcon) in the Treatment of Adults With Acute Bacterial Otitis Externa
Status: Enrolling
Updated: 7/25/2013
Medical Consulting Center
2731
mi
from 98109
Miami, FL
Click here to add this to my saved trials
A Bioequivalence Study of Two Ciprofloxacin/Dexamethasone Formulations in Patients With Otitis Externa
A Randomized, Double-Blind, Placebo-Controlled, Parallel Design, Multiple-Site Study to Evaluate the Clinical Equivalence of Ciprofloxacin 0.3%/Dexamethasone 0.1% Sterile Otic Suspension (Par) Compared to CIPRODEX® (Ciprofloxacin 0.3%/Dexamethasone 0.1%) Sterile Otic Suspension (Alcon) in the Treatment of Adults With Acute Bacterial Otitis Externa
Status: Enrolling
Updated:  7/25/2013
Ormond Medical Arts Pharmaceutical Research Center
2527
mi
from 98109
Ormond Beach, FL
A Bioequivalence Study of Two Ciprofloxacin/Dexamethasone Formulations in Patients With Otitis Externa
A Randomized, Double-Blind, Placebo-Controlled, Parallel Design, Multiple-Site Study to Evaluate the Clinical Equivalence of Ciprofloxacin 0.3%/Dexamethasone 0.1% Sterile Otic Suspension (Par) Compared to CIPRODEX® (Ciprofloxacin 0.3%/Dexamethasone 0.1%) Sterile Otic Suspension (Alcon) in the Treatment of Adults With Acute Bacterial Otitis Externa
Status: Enrolling
Updated: 7/25/2013
Ormond Medical Arts Pharmaceutical Research Center
2527
mi
from 98109
Ormond Beach, FL
Click here to add this to my saved trials
A Bioequivalence Study of Two Ciprofloxacin/Dexamethasone Formulations in Patients With Otitis Externa
A Randomized, Double-Blind, Placebo-Controlled, Parallel Design, Multiple-Site Study to Evaluate the Clinical Equivalence of Ciprofloxacin 0.3%/Dexamethasone 0.1% Sterile Otic Suspension (Par) Compared to CIPRODEX® (Ciprofloxacin 0.3%/Dexamethasone 0.1%) Sterile Otic Suspension (Alcon) in the Treatment of Adults With Acute Bacterial Otitis Externa
Status: Enrolling
Updated:  7/25/2013
Winter Park Clinical Research
2547
mi
from 98109
Winter Park, FL
A Bioequivalence Study of Two Ciprofloxacin/Dexamethasone Formulations in Patients With Otitis Externa
A Randomized, Double-Blind, Placebo-Controlled, Parallel Design, Multiple-Site Study to Evaluate the Clinical Equivalence of Ciprofloxacin 0.3%/Dexamethasone 0.1% Sterile Otic Suspension (Par) Compared to CIPRODEX® (Ciprofloxacin 0.3%/Dexamethasone 0.1%) Sterile Otic Suspension (Alcon) in the Treatment of Adults With Acute Bacterial Otitis Externa
Status: Enrolling
Updated: 7/25/2013
Winter Park Clinical Research
2547
mi
from 98109
Winter Park, FL
Click here to add this to my saved trials
A Bioequivalence Study of Two Ciprofloxacin/Dexamethasone Formulations in Patients With Otitis Externa
A Randomized, Double-Blind, Placebo-Controlled, Parallel Design, Multiple-Site Study to Evaluate the Clinical Equivalence of Ciprofloxacin 0.3%/Dexamethasone 0.1% Sterile Otic Suspension (Par) Compared to CIPRODEX® (Ciprofloxacin 0.3%/Dexamethasone 0.1%) Sterile Otic Suspension (Alcon) in the Treatment of Adults With Acute Bacterial Otitis Externa
Status: Enrolling
Updated:  7/25/2013
Research Integrity, Llc
1896
mi
from 98109
Owensboro, KY
A Bioequivalence Study of Two Ciprofloxacin/Dexamethasone Formulations in Patients With Otitis Externa
A Randomized, Double-Blind, Placebo-Controlled, Parallel Design, Multiple-Site Study to Evaluate the Clinical Equivalence of Ciprofloxacin 0.3%/Dexamethasone 0.1% Sterile Otic Suspension (Par) Compared to CIPRODEX® (Ciprofloxacin 0.3%/Dexamethasone 0.1%) Sterile Otic Suspension (Alcon) in the Treatment of Adults With Acute Bacterial Otitis Externa
Status: Enrolling
Updated: 7/25/2013
Research Integrity, Llc
1896
mi
from 98109
Owensboro, KY
Click here to add this to my saved trials
A Bioequivalence Study of Two Ciprofloxacin/Dexamethasone Formulations in Patients With Otitis Externa
A Randomized, Double-Blind, Placebo-Controlled, Parallel Design, Multiple-Site Study to Evaluate the Clinical Equivalence of Ciprofloxacin 0.3%/Dexamethasone 0.1% Sterile Otic Suspension (Par) Compared to CIPRODEX® (Ciprofloxacin 0.3%/Dexamethasone 0.1%) Sterile Otic Suspension (Alcon) in the Treatment of Adults With Acute Bacterial Otitis Externa
Status: Enrolling
Updated:  7/25/2013
Pioneer Clinical Research, LLC
1372
mi
from 98109
Bellevue, NE
A Bioequivalence Study of Two Ciprofloxacin/Dexamethasone Formulations in Patients With Otitis Externa
A Randomized, Double-Blind, Placebo-Controlled, Parallel Design, Multiple-Site Study to Evaluate the Clinical Equivalence of Ciprofloxacin 0.3%/Dexamethasone 0.1% Sterile Otic Suspension (Par) Compared to CIPRODEX® (Ciprofloxacin 0.3%/Dexamethasone 0.1%) Sterile Otic Suspension (Alcon) in the Treatment of Adults With Acute Bacterial Otitis Externa
Status: Enrolling
Updated: 7/25/2013
Pioneer Clinical Research, LLC
1372
mi
from 98109
Bellevue, NE
Click here to add this to my saved trials
A Bioequivalence Study of Two Ciprofloxacin/Dexamethasone Formulations in Patients With Otitis Externa
A Randomized, Double-Blind, Placebo-Controlled, Parallel Design, Multiple-Site Study to Evaluate the Clinical Equivalence of Ciprofloxacin 0.3%/Dexamethasone 0.1% Sterile Otic Suspension (Par) Compared to CIPRODEX® (Ciprofloxacin 0.3%/Dexamethasone 0.1%) Sterile Otic Suspension (Alcon) in the Treatment of Adults With Acute Bacterial Otitis Externa
Status: Enrolling
Updated:  7/25/2013
PMG Research of Raleigh, LLC
2361
mi
from 98109
Raleigh, NC
A Bioequivalence Study of Two Ciprofloxacin/Dexamethasone Formulations in Patients With Otitis Externa
A Randomized, Double-Blind, Placebo-Controlled, Parallel Design, Multiple-Site Study to Evaluate the Clinical Equivalence of Ciprofloxacin 0.3%/Dexamethasone 0.1% Sterile Otic Suspension (Par) Compared to CIPRODEX® (Ciprofloxacin 0.3%/Dexamethasone 0.1%) Sterile Otic Suspension (Alcon) in the Treatment of Adults With Acute Bacterial Otitis Externa
Status: Enrolling
Updated: 7/25/2013
PMG Research of Raleigh, LLC
2361
mi
from 98109
Raleigh, NC
Click here to add this to my saved trials
A Bioequivalence Study of Two Ciprofloxacin/Dexamethasone Formulations in Patients With Otitis Externa
A Randomized, Double-Blind, Placebo-Controlled, Parallel Design, Multiple-Site Study to Evaluate the Clinical Equivalence of Ciprofloxacin 0.3%/Dexamethasone 0.1% Sterile Otic Suspension (Par) Compared to CIPRODEX® (Ciprofloxacin 0.3%/Dexamethasone 0.1%) Sterile Otic Suspension (Alcon) in the Treatment of Adults With Acute Bacterial Otitis Externa
Status: Enrolling
Updated:  7/25/2013
Pmg Research Of Salisbury
2281
mi
from 98109
Salisbury, NC
A Bioequivalence Study of Two Ciprofloxacin/Dexamethasone Formulations in Patients With Otitis Externa
A Randomized, Double-Blind, Placebo-Controlled, Parallel Design, Multiple-Site Study to Evaluate the Clinical Equivalence of Ciprofloxacin 0.3%/Dexamethasone 0.1% Sterile Otic Suspension (Par) Compared to CIPRODEX® (Ciprofloxacin 0.3%/Dexamethasone 0.1%) Sterile Otic Suspension (Alcon) in the Treatment of Adults With Acute Bacterial Otitis Externa
Status: Enrolling
Updated: 7/25/2013
Pmg Research Of Salisbury
2281
mi
from 98109
Salisbury, NC
Click here to add this to my saved trials
A Bioequivalence Study of Two Ciprofloxacin/Dexamethasone Formulations in Patients With Otitis Externa
A Randomized, Double-Blind, Placebo-Controlled, Parallel Design, Multiple-Site Study to Evaluate the Clinical Equivalence of Ciprofloxacin 0.3%/Dexamethasone 0.1% Sterile Otic Suspension (Par) Compared to CIPRODEX® (Ciprofloxacin 0.3%/Dexamethasone 0.1%) Sterile Otic Suspension (Alcon) in the Treatment of Adults With Acute Bacterial Otitis Externa
Status: Enrolling
Updated:  7/25/2013
Julia Mullen, MD
1963
mi
from 98109
Cincinnati, OH
A Bioequivalence Study of Two Ciprofloxacin/Dexamethasone Formulations in Patients With Otitis Externa
A Randomized, Double-Blind, Placebo-Controlled, Parallel Design, Multiple-Site Study to Evaluate the Clinical Equivalence of Ciprofloxacin 0.3%/Dexamethasone 0.1% Sterile Otic Suspension (Par) Compared to CIPRODEX® (Ciprofloxacin 0.3%/Dexamethasone 0.1%) Sterile Otic Suspension (Alcon) in the Treatment of Adults With Acute Bacterial Otitis Externa
Status: Enrolling
Updated: 7/25/2013
Julia Mullen, MD
1963
mi
from 98109
Cincinnati, OH
Click here to add this to my saved trials
A Bioequivalence Study of Two Ciprofloxacin/Dexamethasone Formulations in Patients With Otitis Externa
A Randomized, Double-Blind, Placebo-Controlled, Parallel Design, Multiple-Site Study to Evaluate the Clinical Equivalence of Ciprofloxacin 0.3%/Dexamethasone 0.1% Sterile Otic Suspension (Par) Compared to CIPRODEX® (Ciprofloxacin 0.3%/Dexamethasone 0.1%) Sterile Otic Suspension (Alcon) in the Treatment of Adults With Acute Bacterial Otitis Externa
Status: Enrolling
Updated:  7/25/2013
Integrated Medical Research, PC
375
mi
from 98109
Ashland, OR
A Bioequivalence Study of Two Ciprofloxacin/Dexamethasone Formulations in Patients With Otitis Externa
A Randomized, Double-Blind, Placebo-Controlled, Parallel Design, Multiple-Site Study to Evaluate the Clinical Equivalence of Ciprofloxacin 0.3%/Dexamethasone 0.1% Sterile Otic Suspension (Par) Compared to CIPRODEX® (Ciprofloxacin 0.3%/Dexamethasone 0.1%) Sterile Otic Suspension (Alcon) in the Treatment of Adults With Acute Bacterial Otitis Externa
Status: Enrolling
Updated: 7/25/2013
Integrated Medical Research, PC
375
mi
from 98109
Ashland, OR
Click here to add this to my saved trials
A Bioequivalence Study of Two Ciprofloxacin/Dexamethasone Formulations in Patients With Otitis Externa
A Randomized, Double-Blind, Placebo-Controlled, Parallel Design, Multiple-Site Study to Evaluate the Clinical Equivalence of Ciprofloxacin 0.3%/Dexamethasone 0.1% Sterile Otic Suspension (Par) Compared to CIPRODEX® (Ciprofloxacin 0.3%/Dexamethasone 0.1%) Sterile Otic Suspension (Alcon) in the Treatment of Adults With Acute Bacterial Otitis Externa
Status: Enrolling
Updated:  7/25/2013
Cyn3rgy
146
mi
from 98109
Gresham, OR
A Bioequivalence Study of Two Ciprofloxacin/Dexamethasone Formulations in Patients With Otitis Externa
A Randomized, Double-Blind, Placebo-Controlled, Parallel Design, Multiple-Site Study to Evaluate the Clinical Equivalence of Ciprofloxacin 0.3%/Dexamethasone 0.1% Sterile Otic Suspension (Par) Compared to CIPRODEX® (Ciprofloxacin 0.3%/Dexamethasone 0.1%) Sterile Otic Suspension (Alcon) in the Treatment of Adults With Acute Bacterial Otitis Externa
Status: Enrolling
Updated: 7/25/2013
Cyn3rgy
146
mi
from 98109
Gresham, OR
Click here to add this to my saved trials
A Bioequivalence Study of Two Ciprofloxacin/Dexamethasone Formulations in Patients With Otitis Externa
A Randomized, Double-Blind, Placebo-Controlled, Parallel Design, Multiple-Site Study to Evaluate the Clinical Equivalence of Ciprofloxacin 0.3%/Dexamethasone 0.1% Sterile Otic Suspension (Par) Compared to CIPRODEX® (Ciprofloxacin 0.3%/Dexamethasone 0.1%) Sterile Otic Suspension (Alcon) in the Treatment of Adults With Acute Bacterial Otitis Externa
Status: Enrolling
Updated:  7/25/2013
PEAK Research LLC
2132
mi
from 98109
Upper St. Clair, PA
A Bioequivalence Study of Two Ciprofloxacin/Dexamethasone Formulations in Patients With Otitis Externa
A Randomized, Double-Blind, Placebo-Controlled, Parallel Design, Multiple-Site Study to Evaluate the Clinical Equivalence of Ciprofloxacin 0.3%/Dexamethasone 0.1% Sterile Otic Suspension (Par) Compared to CIPRODEX® (Ciprofloxacin 0.3%/Dexamethasone 0.1%) Sterile Otic Suspension (Alcon) in the Treatment of Adults With Acute Bacterial Otitis Externa
Status: Enrolling
Updated: 7/25/2013
PEAK Research LLC
2132
mi
from 98109
Upper St. Clair, PA
Click here to add this to my saved trials
A Bioequivalence Study of Two Ciprofloxacin/Dexamethasone Formulations in Patients With Otitis Externa
A Randomized, Double-Blind, Placebo-Controlled, Parallel Design, Multiple-Site Study to Evaluate the Clinical Equivalence of Ciprofloxacin 0.3%/Dexamethasone 0.1% Sterile Otic Suspension (Par) Compared to CIPRODEX® (Ciprofloxacin 0.3%/Dexamethasone 0.1%) Sterile Otic Suspension (Alcon) in the Treatment of Adults With Acute Bacterial Otitis Externa
Status: Enrolling
Updated:  7/25/2013
John Ansley, MD
2347
mi
from 98109
Orangeburgh, SC
A Bioequivalence Study of Two Ciprofloxacin/Dexamethasone Formulations in Patients With Otitis Externa
A Randomized, Double-Blind, Placebo-Controlled, Parallel Design, Multiple-Site Study to Evaluate the Clinical Equivalence of Ciprofloxacin 0.3%/Dexamethasone 0.1% Sterile Otic Suspension (Par) Compared to CIPRODEX® (Ciprofloxacin 0.3%/Dexamethasone 0.1%) Sterile Otic Suspension (Alcon) in the Treatment of Adults With Acute Bacterial Otitis Externa
Status: Enrolling
Updated: 7/25/2013
John Ansley, MD
2347
mi
from 98109
Orangeburgh, SC
Click here to add this to my saved trials
A Bioequivalence Study of Two Ciprofloxacin/Dexamethasone Formulations in Patients With Otitis Externa
A Randomized, Double-Blind, Placebo-Controlled, Parallel Design, Multiple-Site Study to Evaluate the Clinical Equivalence of Ciprofloxacin 0.3%/Dexamethasone 0.1% Sterile Otic Suspension (Par) Compared to CIPRODEX® (Ciprofloxacin 0.3%/Dexamethasone 0.1%) Sterile Otic Suspension (Alcon) in the Treatment of Adults With Acute Bacterial Otitis Externa
Status: Enrolling
Updated:  7/25/2013
Spartanburg and Geer ENT
2240
mi
from 98109
Spartanburg, SC
A Bioequivalence Study of Two Ciprofloxacin/Dexamethasone Formulations in Patients With Otitis Externa
A Randomized, Double-Blind, Placebo-Controlled, Parallel Design, Multiple-Site Study to Evaluate the Clinical Equivalence of Ciprofloxacin 0.3%/Dexamethasone 0.1% Sterile Otic Suspension (Par) Compared to CIPRODEX® (Ciprofloxacin 0.3%/Dexamethasone 0.1%) Sterile Otic Suspension (Alcon) in the Treatment of Adults With Acute Bacterial Otitis Externa
Status: Enrolling
Updated: 7/25/2013
Spartanburg and Geer ENT
2240
mi
from 98109
Spartanburg, SC
Click here to add this to my saved trials
A Bioequivalence Study of Two Ciprofloxacin/Dexamethasone Formulations in Patients With Otitis Externa
A Randomized, Double-Blind, Placebo-Controlled, Parallel Design, Multiple-Site Study to Evaluate the Clinical Equivalence of Ciprofloxacin 0.3%/Dexamethasone 0.1% Sterile Otic Suspension (Par) Compared to CIPRODEX® (Ciprofloxacin 0.3%/Dexamethasone 0.1%) Sterile Otic Suspension (Alcon) in the Treatment of Adults With Acute Bacterial Otitis Externa
Status: Enrolling
Updated:  7/25/2013
Monica Davis, MD
1976
mi
from 98109
Brentwood, TN
A Bioequivalence Study of Two Ciprofloxacin/Dexamethasone Formulations in Patients With Otitis Externa
A Randomized, Double-Blind, Placebo-Controlled, Parallel Design, Multiple-Site Study to Evaluate the Clinical Equivalence of Ciprofloxacin 0.3%/Dexamethasone 0.1% Sterile Otic Suspension (Par) Compared to CIPRODEX® (Ciprofloxacin 0.3%/Dexamethasone 0.1%) Sterile Otic Suspension (Alcon) in the Treatment of Adults With Acute Bacterial Otitis Externa
Status: Enrolling
Updated: 7/25/2013
Monica Davis, MD
1976
mi
from 98109
Brentwood, TN
Click here to add this to my saved trials
A Bioequivalence Study of Two Ciprofloxacin/Dexamethasone Formulations in Patients With Otitis Externa
A Randomized, Double-Blind, Placebo-Controlled, Parallel Design, Multiple-Site Study to Evaluate the Clinical Equivalence of Ciprofloxacin 0.3%/Dexamethasone 0.1% Sterile Otic Suspension (Par) Compared to CIPRODEX® (Ciprofloxacin 0.3%/Dexamethasone 0.1%) Sterile Otic Suspension (Alcon) in the Treatment of Adults With Acute Bacterial Otitis Externa
Status: Enrolling
Updated:  7/25/2013
Gilbert Ledesma, MD
1667
mi
from 98109
Arlington, TX
A Bioequivalence Study of Two Ciprofloxacin/Dexamethasone Formulations in Patients With Otitis Externa
A Randomized, Double-Blind, Placebo-Controlled, Parallel Design, Multiple-Site Study to Evaluate the Clinical Equivalence of Ciprofloxacin 0.3%/Dexamethasone 0.1% Sterile Otic Suspension (Par) Compared to CIPRODEX® (Ciprofloxacin 0.3%/Dexamethasone 0.1%) Sterile Otic Suspension (Alcon) in the Treatment of Adults With Acute Bacterial Otitis Externa
Status: Enrolling
Updated: 7/25/2013
Gilbert Ledesma, MD
1667
mi
from 98109
Arlington, TX
Click here to add this to my saved trials
A Bioequivalence Study of Two Ciprofloxacin/Dexamethasone Formulations in Patients With Otitis Externa
A Randomized, Double-Blind, Placebo-Controlled, Parallel Design, Multiple-Site Study to Evaluate the Clinical Equivalence of Ciprofloxacin 0.3%/Dexamethasone 0.1% Sterile Otic Suspension (Par) Compared to CIPRODEX® (Ciprofloxacin 0.3%/Dexamethasone 0.1%) Sterile Otic Suspension (Alcon) in the Treatment of Adults With Acute Bacterial Otitis Externa
Status: Enrolling
Updated:  7/25/2013
West Houston Clinical Research Service
1883
mi
from 98109
Houston, TX
A Bioequivalence Study of Two Ciprofloxacin/Dexamethasone Formulations in Patients With Otitis Externa
A Randomized, Double-Blind, Placebo-Controlled, Parallel Design, Multiple-Site Study to Evaluate the Clinical Equivalence of Ciprofloxacin 0.3%/Dexamethasone 0.1% Sterile Otic Suspension (Par) Compared to CIPRODEX® (Ciprofloxacin 0.3%/Dexamethasone 0.1%) Sterile Otic Suspension (Alcon) in the Treatment of Adults With Acute Bacterial Otitis Externa
Status: Enrolling
Updated: 7/25/2013
West Houston Clinical Research Service
1883
mi
from 98109
Houston, TX
Click here to add this to my saved trials
A Bioequivalence Study of Two Ciprofloxacin/Dexamethasone Formulations in Patients With Otitis Externa
A Randomized, Double-Blind, Placebo-Controlled, Parallel Design, Multiple-Site Study to Evaluate the Clinical Equivalence of Ciprofloxacin 0.3%/Dexamethasone 0.1% Sterile Otic Suspension (Par) Compared to CIPRODEX® (Ciprofloxacin 0.3%/Dexamethasone 0.1%) Sterile Otic Suspension (Alcon) in the Treatment of Adults With Acute Bacterial Otitis Externa
Status: Enrolling
Updated:  7/25/2013
R/D Clinical Research, Inc.
1925
mi
from 98109
Lake Jackson, TX
A Bioequivalence Study of Two Ciprofloxacin/Dexamethasone Formulations in Patients With Otitis Externa
A Randomized, Double-Blind, Placebo-Controlled, Parallel Design, Multiple-Site Study to Evaluate the Clinical Equivalence of Ciprofloxacin 0.3%/Dexamethasone 0.1% Sterile Otic Suspension (Par) Compared to CIPRODEX® (Ciprofloxacin 0.3%/Dexamethasone 0.1%) Sterile Otic Suspension (Alcon) in the Treatment of Adults With Acute Bacterial Otitis Externa
Status: Enrolling
Updated: 7/25/2013
R/D Clinical Research, Inc.
1925
mi
from 98109
Lake Jackson, TX
Click here to add this to my saved trials
A Bioequivalence Study of Two Ciprofloxacin/Dexamethasone Formulations in Patients With Otitis Externa
A Randomized, Double-Blind, Placebo-Controlled, Parallel Design, Multiple-Site Study to Evaluate the Clinical Equivalence of Ciprofloxacin 0.3%/Dexamethasone 0.1% Sterile Otic Suspension (Par) Compared to CIPRODEX® (Ciprofloxacin 0.3%/Dexamethasone 0.1%) Sterile Otic Suspension (Alcon) in the Treatment of Adults With Acute Bacterial Otitis Externa
Status: Enrolling
Updated:  7/25/2013
The Education and Research Foundation, Inc.
2275
mi
from 98109
Lynchburg, VA
A Bioequivalence Study of Two Ciprofloxacin/Dexamethasone Formulations in Patients With Otitis Externa
A Randomized, Double-Blind, Placebo-Controlled, Parallel Design, Multiple-Site Study to Evaluate the Clinical Equivalence of Ciprofloxacin 0.3%/Dexamethasone 0.1% Sterile Otic Suspension (Par) Compared to CIPRODEX® (Ciprofloxacin 0.3%/Dexamethasone 0.1%) Sterile Otic Suspension (Alcon) in the Treatment of Adults With Acute Bacterial Otitis Externa
Status: Enrolling
Updated: 7/25/2013
The Education and Research Foundation, Inc.
2275
mi
from 98109
Lynchburg, VA
Click here to add this to my saved trials
A Study To Evaluate The Safety Of Voriconazole As Treatment Of Invasive Aspergillosis (Fungal Infection) And Other Rare Molds In Children
A Prospective, Open-Label, Non-Randomized, Multi-Center Study To Investigate The Safety And Tolerability Of Voriconazole As Primary Therapy For Treatment Of Invasive Aspergillosis And Molds Such As Scedosporium Or Fusarium Species In Pediatric Patients
Status: Enrolling
Updated:  7/31/2013
Pfizer Investigational Site
979
mi
from 98109
Los Angeles, CA
A Study To Evaluate The Safety Of Voriconazole As Treatment Of Invasive Aspergillosis (Fungal Infection) And Other Rare Molds In Children
A Prospective, Open-Label, Non-Randomized, Multi-Center Study To Investigate The Safety And Tolerability Of Voriconazole As Primary Therapy For Treatment Of Invasive Aspergillosis And Molds Such As Scedosporium Or Fusarium Species In Pediatric Patients
Status: Enrolling
Updated: 7/31/2013
Pfizer Investigational Site
979
mi
from 98109
Los Angeles, CA
Click here to add this to my saved trials
A Study To Evaluate The Safety Of Voriconazole As Treatment Of Invasive Aspergillosis (Fungal Infection) And Other Rare Molds In Children
A Prospective, Open-Label, Non-Randomized, Multi-Center Study To Investigate The Safety And Tolerability Of Voriconazole As Primary Therapy For Treatment Of Invasive Aspergillosis And Molds Such As Scedosporium Or Fusarium Species In Pediatric Patients
Status: Enrolling
Updated:  7/31/2013
Pfizer Investigational Site
2125
mi
from 98109
Biloxi, MS
A Study To Evaluate The Safety Of Voriconazole As Treatment Of Invasive Aspergillosis (Fungal Infection) And Other Rare Molds In Children
A Prospective, Open-Label, Non-Randomized, Multi-Center Study To Investigate The Safety And Tolerability Of Voriconazole As Primary Therapy For Treatment Of Invasive Aspergillosis And Molds Such As Scedosporium Or Fusarium Species In Pediatric Patients
Status: Enrolling
Updated: 7/31/2013
Pfizer Investigational Site
2125
mi
from 98109
Biloxi, MS
Click here to add this to my saved trials
A Study To Evaluate The Safety Of Voriconazole As Treatment Of Invasive Aspergillosis (Fungal Infection) And Other Rare Molds In Children
A Prospective, Open-Label, Non-Randomized, Multi-Center Study To Investigate The Safety And Tolerability Of Voriconazole As Primary Therapy For Treatment Of Invasive Aspergillosis And Molds Such As Scedosporium Or Fusarium Species In Pediatric Patients
Status: Enrolling
Updated:  7/31/2013
Pfizer Investigational Site
2131
mi
from 98109
Pittsburgh, PA
A Study To Evaluate The Safety Of Voriconazole As Treatment Of Invasive Aspergillosis (Fungal Infection) And Other Rare Molds In Children
A Prospective, Open-Label, Non-Randomized, Multi-Center Study To Investigate The Safety And Tolerability Of Voriconazole As Primary Therapy For Treatment Of Invasive Aspergillosis And Molds Such As Scedosporium Or Fusarium Species In Pediatric Patients
Status: Enrolling
Updated: 7/31/2013
Pfizer Investigational Site
2131
mi
from 98109
Pittsburgh, PA
Click here to add this to my saved trials
A Study To Evaluate The Safety Of Voriconazole As Treatment Of Invasive Aspergillosis (Fungal Infection) And Other Rare Molds In Children
A Prospective, Open-Label, Non-Randomized, Multi-Center Study To Investigate The Safety And Tolerability Of Voriconazole As Primary Therapy For Treatment Of Invasive Aspergillosis And Molds Such As Scedosporium Or Fusarium Species In Pediatric Patients
Status: Enrolling
Updated:  7/31/2013
Pfizer Investigational Site
1892
mi
from 98109
Houston, TX
A Study To Evaluate The Safety Of Voriconazole As Treatment Of Invasive Aspergillosis (Fungal Infection) And Other Rare Molds In Children
A Prospective, Open-Label, Non-Randomized, Multi-Center Study To Investigate The Safety And Tolerability Of Voriconazole As Primary Therapy For Treatment Of Invasive Aspergillosis And Molds Such As Scedosporium Or Fusarium Species In Pediatric Patients
Status: Enrolling
Updated: 7/31/2013
Pfizer Investigational Site
1892
mi
from 98109
Houston, TX
Click here to add this to my saved trials
A Study To Evaluate The Safety Of Voriconazole As Treatment Of Invasive Aspergillosis (Fungal Infection) And Other Rare Molds In Children
A Prospective, Open-Label, Non-Randomized, Multi-Center Study To Investigate The Safety And Tolerability Of Voriconazole As Primary Therapy For Treatment Of Invasive Aspergillosis And Molds Such As Scedosporium Or Fusarium Species In Pediatric Patients
Status: Enrolling
Updated:  7/31/2013
Pfizer Investigational Site
2314
mi
from 98109
Burke, VA
A Study To Evaluate The Safety Of Voriconazole As Treatment Of Invasive Aspergillosis (Fungal Infection) And Other Rare Molds In Children
A Prospective, Open-Label, Non-Randomized, Multi-Center Study To Investigate The Safety And Tolerability Of Voriconazole As Primary Therapy For Treatment Of Invasive Aspergillosis And Molds Such As Scedosporium Or Fusarium Species In Pediatric Patients
Status: Enrolling
Updated: 7/31/2013
Pfizer Investigational Site
2314
mi
from 98109
Burke, VA
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Assessing Fever Rates in Children Ages 24 to 59 Months After Live Attenuated Influenza Vaccine (LAIV) or Inactivated Influenza Vaccines (IIV) Using Text Messaging for U.S. Influenza Vaccines in 2012-2013 & 2013-2014
Assessing Fever Rates in Children Ages 24 to 59 Months After Live Attenuated Influenza Vaccine (LAIV) or Inactivated Influenza Vaccines (IIV) Using Text Messaging for U.S. Influenza Vaccines in 2012-2013 & 2013-2014
Status: Enrolling
Updated:  8/1/2013
Centers for Disease Control and Prevention
2187
mi
from 98109
Atlanta, GA
Assessing Fever Rates in Children Ages 24 to 59 Months After Live Attenuated Influenza Vaccine (LAIV) or Inactivated Influenza Vaccines (IIV) Using Text Messaging for U.S. Influenza Vaccines in 2012-2013 & 2013-2014
Assessing Fever Rates in Children Ages 24 to 59 Months After Live Attenuated Influenza Vaccine (LAIV) or Inactivated Influenza Vaccines (IIV) Using Text Messaging for U.S. Influenza Vaccines in 2012-2013 & 2013-2014
Status: Enrolling
Updated: 8/1/2013
Centers for Disease Control and Prevention
2187
mi
from 98109
Atlanta, GA
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Assessing Fever Rates in Children Ages 24 to 59 Months After Live Attenuated Influenza Vaccine (LAIV) or Inactivated Influenza Vaccines (IIV) Using Text Messaging for U.S. Influenza Vaccines in 2012-2013 & 2013-2014
Assessing Fever Rates in Children Ages 24 to 59 Months After Live Attenuated Influenza Vaccine (LAIV) or Inactivated Influenza Vaccines (IIV) Using Text Messaging for U.S. Influenza Vaccines in 2012-2013 & 2013-2014
Status: Enrolling
Updated:  8/1/2013
Columbia University
2400
mi
from 98109
New York, NY
Assessing Fever Rates in Children Ages 24 to 59 Months After Live Attenuated Influenza Vaccine (LAIV) or Inactivated Influenza Vaccines (IIV) Using Text Messaging for U.S. Influenza Vaccines in 2012-2013 & 2013-2014
Assessing Fever Rates in Children Ages 24 to 59 Months After Live Attenuated Influenza Vaccine (LAIV) or Inactivated Influenza Vaccines (IIV) Using Text Messaging for U.S. Influenza Vaccines in 2012-2013 & 2013-2014
Status: Enrolling
Updated: 8/1/2013
Columbia University
2400
mi
from 98109
New York, NY
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A Safety and Tolerability Study of Doripenem Compared With Meropenem in Children Hospitalized With Complicated Intra-abdominal Infections
A Prospective, Randomized, Double-Blind, Multicenter Study to Establish the Safety and Tolerability of Doripenem Compared With Meropenem in Hospitalized Children With Complicated Intra-Abdominal Infections
Status: Enrolling
Updated:  8/6/2013
Clinical Research Facility
710
mi
from 98109
Santa Clara, CA
A Safety and Tolerability Study of Doripenem Compared With Meropenem in Children Hospitalized With Complicated Intra-abdominal Infections
A Prospective, Randomized, Double-Blind, Multicenter Study to Establish the Safety and Tolerability of Doripenem Compared With Meropenem in Hospitalized Children With Complicated Intra-Abdominal Infections
Status: Enrolling
Updated: 8/6/2013
Clinical Research Facility
710
mi
from 98109
Santa Clara, CA
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A Safety and Tolerability Study of Doripenem Compared With Meropenem in Children Hospitalized With Complicated Intra-abdominal Infections
A Prospective, Randomized, Double-Blind, Multicenter Study to Establish the Safety and Tolerability of Doripenem Compared With Meropenem in Hospitalized Children With Complicated Intra-Abdominal Infections
Status: Enrolling
Updated:  8/6/2013
Clinical Research Facility
1026
mi
from 98109
Aurora, CO
A Safety and Tolerability Study of Doripenem Compared With Meropenem in Children Hospitalized With Complicated Intra-abdominal Infections
A Prospective, Randomized, Double-Blind, Multicenter Study to Establish the Safety and Tolerability of Doripenem Compared With Meropenem in Hospitalized Children With Complicated Intra-Abdominal Infections
Status: Enrolling
Updated: 8/6/2013
Clinical Research Facility
1026
mi
from 98109
Aurora, CO
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A Safety and Tolerability Study of Doripenem Compared With Meropenem in Children Hospitalized With Complicated Intra-abdominal Infections
A Prospective, Randomized, Double-Blind, Multicenter Study to Establish the Safety and Tolerability of Doripenem Compared With Meropenem in Hospitalized Children With Complicated Intra-Abdominal Infections
Status: Enrolling
Updated:  8/6/2013
Clinical Research Facility
2322
mi
from 98109
Washington,
A Safety and Tolerability Study of Doripenem Compared With Meropenem in Children Hospitalized With Complicated Intra-abdominal Infections
A Prospective, Randomized, Double-Blind, Multicenter Study to Establish the Safety and Tolerability of Doripenem Compared With Meropenem in Hospitalized Children With Complicated Intra-Abdominal Infections
Status: Enrolling
Updated: 8/6/2013
Clinical Research Facility
2322
mi
from 98109
Washington,
Click here to add this to my saved trials
A Safety and Tolerability Study of Doripenem Compared With Meropenem in Children Hospitalized With Complicated Intra-abdominal Infections
A Prospective, Randomized, Double-Blind, Multicenter Study to Establish the Safety and Tolerability of Doripenem Compared With Meropenem in Hospitalized Children With Complicated Intra-Abdominal Infections
Status: Enrolling
Updated:  8/6/2013
Clinical Research Facility
1719
mi
from 98109
Park Ridge, IL
A Safety and Tolerability Study of Doripenem Compared With Meropenem in Children Hospitalized With Complicated Intra-abdominal Infections
A Prospective, Randomized, Double-Blind, Multicenter Study to Establish the Safety and Tolerability of Doripenem Compared With Meropenem in Hospitalized Children With Complicated Intra-Abdominal Infections
Status: Enrolling
Updated: 8/6/2013
Clinical Research Facility
1719
mi
from 98109
Park Ridge, IL
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A Safety and Tolerability Study of Doripenem Compared With Meropenem in Children Hospitalized With Complicated Intra-abdominal Infections
A Prospective, Randomized, Double-Blind, Multicenter Study to Establish the Safety and Tolerability of Doripenem Compared With Meropenem in Hospitalized Children With Complicated Intra-Abdominal Infections
Status: Enrolling
Updated:  8/6/2013
Clinical Research Facility
1939
mi
from 98109
Louisville, KY
A Safety and Tolerability Study of Doripenem Compared With Meropenem in Children Hospitalized With Complicated Intra-abdominal Infections
A Prospective, Randomized, Double-Blind, Multicenter Study to Establish the Safety and Tolerability of Doripenem Compared With Meropenem in Hospitalized Children With Complicated Intra-Abdominal Infections
Status: Enrolling
Updated: 8/6/2013
Clinical Research Facility
1939
mi
from 98109
Louisville, KY
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A Safety and Tolerability Study of Doripenem Compared With Meropenem in Children Hospitalized With Complicated Intra-abdominal Infections
A Prospective, Randomized, Double-Blind, Multicenter Study to Establish the Safety and Tolerability of Doripenem Compared With Meropenem in Hospitalized Children With Complicated Intra-Abdominal Infections
Status: Enrolling
Updated:  8/6/2013
Clinical Research Facility
2091
mi
from 98109
Metairie, LA
A Safety and Tolerability Study of Doripenem Compared With Meropenem in Children Hospitalized With Complicated Intra-abdominal Infections
A Prospective, Randomized, Double-Blind, Multicenter Study to Establish the Safety and Tolerability of Doripenem Compared With Meropenem in Hospitalized Children With Complicated Intra-Abdominal Infections
Status: Enrolling
Updated: 8/6/2013
Clinical Research Facility
2091
mi
from 98109
Metairie, LA
Click here to add this to my saved trials
A Safety and Tolerability Study of Doripenem Compared With Meropenem in Children Hospitalized With Complicated Intra-abdominal Infections
A Prospective, Randomized, Double-Blind, Multicenter Study to Establish the Safety and Tolerability of Doripenem Compared With Meropenem in Hospitalized Children With Complicated Intra-Abdominal Infections
Status: Enrolling
Updated:  8/6/2013
Clinical Research Facility
2485
mi
from 98109
Boston, MA
A Safety and Tolerability Study of Doripenem Compared With Meropenem in Children Hospitalized With Complicated Intra-abdominal Infections
A Prospective, Randomized, Double-Blind, Multicenter Study to Establish the Safety and Tolerability of Doripenem Compared With Meropenem in Hospitalized Children With Complicated Intra-Abdominal Infections
Status: Enrolling
Updated: 8/6/2013
Clinical Research Facility
2485
mi
from 98109
Boston, MA
Click here to add this to my saved trials
A Safety and Tolerability Study of Doripenem Compared With Meropenem in Children Hospitalized With Complicated Intra-abdominal Infections
A Prospective, Randomized, Double-Blind, Multicenter Study to Establish the Safety and Tolerability of Doripenem Compared With Meropenem in Hospitalized Children With Complicated Intra-Abdominal Infections
Status: Enrolling
Updated:  8/6/2013
Clinical Research Facility
1903
mi
from 98109
Ann Arbor, MI
A Safety and Tolerability Study of Doripenem Compared With Meropenem in Children Hospitalized With Complicated Intra-abdominal Infections
A Prospective, Randomized, Double-Blind, Multicenter Study to Establish the Safety and Tolerability of Doripenem Compared With Meropenem in Hospitalized Children With Complicated Intra-Abdominal Infections
Status: Enrolling
Updated: 8/6/2013
Clinical Research Facility
1903
mi
from 98109
Ann Arbor, MI
Click here to add this to my saved trials
A Safety and Tolerability Study of Doripenem Compared With Meropenem in Children Hospitalized With Complicated Intra-abdominal Infections
A Prospective, Randomized, Double-Blind, Multicenter Study to Establish the Safety and Tolerability of Doripenem Compared With Meropenem in Hospitalized Children With Complicated Intra-Abdominal Infections
Status: Enrolling
Updated:  8/6/2013
Clinical Research Facility
2400
mi
from 98109
New York, NY
A Safety and Tolerability Study of Doripenem Compared With Meropenem in Children Hospitalized With Complicated Intra-abdominal Infections
A Prospective, Randomized, Double-Blind, Multicenter Study to Establish the Safety and Tolerability of Doripenem Compared With Meropenem in Hospitalized Children With Complicated Intra-Abdominal Infections
Status: Enrolling
Updated: 8/6/2013
Clinical Research Facility
2400
mi
from 98109
New York, NY
Click here to add this to my saved trials
A Safety and Tolerability Study of Doripenem Compared With Meropenem in Children Hospitalized With Complicated Intra-abdominal Infections
A Prospective, Randomized, Double-Blind, Multicenter Study to Establish the Safety and Tolerability of Doripenem Compared With Meropenem in Hospitalized Children With Complicated Intra-Abdominal Infections
Status: Enrolling
Updated:  8/6/2013
Clinical Research Facility
2020
mi
from 98109
Cleveland, OH
A Safety and Tolerability Study of Doripenem Compared With Meropenem in Children Hospitalized With Complicated Intra-abdominal Infections
A Prospective, Randomized, Double-Blind, Multicenter Study to Establish the Safety and Tolerability of Doripenem Compared With Meropenem in Hospitalized Children With Complicated Intra-Abdominal Infections
Status: Enrolling
Updated: 8/6/2013
Clinical Research Facility
2020
mi
from 98109
Cleveland, OH
Click here to add this to my saved trials
A Safety and Tolerability Study of Doripenem Compared With Meropenem in Children Hospitalized With Complicated Intra-abdominal Infections
A Prospective, Randomized, Double-Blind, Multicenter Study to Establish the Safety and Tolerability of Doripenem Compared With Meropenem in Hospitalized Children With Complicated Intra-Abdominal Infections
Status: Enrolling
Updated:  8/6/2013
Clinical Research Facility
2373
mi
from 98109
Philadelphia, PA
A Safety and Tolerability Study of Doripenem Compared With Meropenem in Children Hospitalized With Complicated Intra-abdominal Infections
A Prospective, Randomized, Double-Blind, Multicenter Study to Establish the Safety and Tolerability of Doripenem Compared With Meropenem in Hospitalized Children With Complicated Intra-Abdominal Infections
Status: Enrolling
Updated: 8/6/2013
Clinical Research Facility
2373
mi
from 98109
Philadelphia, PA
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Fecal Microbiota Transplant for Relapsing Clostridium Difficile Infection in Adults and Children Using a Frozen Encapsulated Inoculum
Fecal Microbiota Transplant (FMT) for Relapsing Clostridium Difficile Infection in Adults and Children Using a Frozen Encapsulated Inoculum
Status: Enrolling
Updated:  8/6/2013
Massachusetts General Hospital
2485
mi
from 98109
Boston, MA
Fecal Microbiota Transplant for Relapsing Clostridium Difficile Infection in Adults and Children Using a Frozen Encapsulated Inoculum
Fecal Microbiota Transplant (FMT) for Relapsing Clostridium Difficile Infection in Adults and Children Using a Frozen Encapsulated Inoculum
Status: Enrolling
Updated: 8/6/2013
Massachusetts General Hospital
2485
mi
from 98109
Boston, MA
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Expanding Antimicrobial Stewardship
Expanding Antimicrobial Stewardship
Status: Enrolling
Updated:  8/12/2013
Wexner Medical Center at the Ohio State University
2008
mi
from 98109
Columbus, OH
Expanding Antimicrobial Stewardship
Expanding Antimicrobial Stewardship
Status: Enrolling
Updated: 8/12/2013
Wexner Medical Center at the Ohio State University
2008
mi
from 98109
Columbus, OH
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Hepatic Encephalopathy: Lactulose or Polyethylene Glycol (H.E.L.P.)
Hepatic Encephalopathy: Lactulose or Polyethylene Glycol (H.E.L.P.)
Status: Enrolling
Updated:  8/13/2013
New York Methodist Hospital
2404
mi
from 98109
Brooklyn, NY
Hepatic Encephalopathy: Lactulose or Polyethylene Glycol (H.E.L.P.)
Hepatic Encephalopathy: Lactulose or Polyethylene Glycol (H.E.L.P.)
Status: Enrolling
Updated: 8/13/2013
New York Methodist Hospital
2404
mi
from 98109
Brooklyn, NY
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Anal Dysplasia Study of Men Who Have Sex With Men Living With HIV
Anal Dysplasia Study of Men Who Have Sex With Men Living With HIV
Status: Enrolling
Updated:  8/15/2013
NMCSD
1065
mi
from 98109
San Diego, CA
Anal Dysplasia Study of Men Who Have Sex With Men Living With HIV
Anal Dysplasia Study of Men Who Have Sex With Men Living With HIV
Status: Enrolling
Updated: 8/15/2013
NMCSD
1065
mi
from 98109
San Diego, CA
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Darbe Administration in Newborns Undergoing Cooling for Encephalopathy
Darbe Administration in Newborns Undergoing Cooling for Encephalopathy
Status: Enrolling
Updated:  8/26/2013
University of New Mexico
1186
mi
from 98109
Albuquerque, NM
Darbe Administration in Newborns Undergoing Cooling for Encephalopathy
Darbe Administration in Newborns Undergoing Cooling for Encephalopathy
Status: Enrolling
Updated: 8/26/2013
University of New Mexico
1186
mi
from 98109
Albuquerque, NM
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Darbe Administration in Newborns Undergoing Cooling for Encephalopathy
Darbe Administration in Newborns Undergoing Cooling for Encephalopathy
Status: Enrolling
Updated:  8/26/2013
Vanderbilt University School of Medicine
1970
mi
from 98109
Nashville, TN
Darbe Administration in Newborns Undergoing Cooling for Encephalopathy
Darbe Administration in Newborns Undergoing Cooling for Encephalopathy
Status: Enrolling
Updated: 8/26/2013
Vanderbilt University School of Medicine
1970
mi
from 98109
Nashville, TN
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Darbe Administration in Newborns Undergoing Cooling for Encephalopathy
Darbe Administration in Newborns Undergoing Cooling for Encephalopathy
Status: Enrolling
Updated:  8/26/2013
McKay Dee Hospital- Intermountain Healthcare
675
mi
from 98109
Ogden, UT
Darbe Administration in Newborns Undergoing Cooling for Encephalopathy
Darbe Administration in Newborns Undergoing Cooling for Encephalopathy
Status: Enrolling
Updated: 8/26/2013
McKay Dee Hospital- Intermountain Healthcare
675
mi
from 98109
Ogden, UT
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Darbe Administration in Newborns Undergoing Cooling for Encephalopathy
Darbe Administration in Newborns Undergoing Cooling for Encephalopathy
Status: Enrolling
Updated:  8/26/2013
Primary Children's Hospital
699
mi
from 98109
Salt Lake City, UT
Darbe Administration in Newborns Undergoing Cooling for Encephalopathy
Darbe Administration in Newborns Undergoing Cooling for Encephalopathy
Status: Enrolling
Updated: 8/26/2013
Primary Children's Hospital
699
mi
from 98109
Salt Lake City, UT
Click here to add this to my saved trials
Darbe Administration in Newborns Undergoing Cooling for Encephalopathy
Darbe Administration in Newborns Undergoing Cooling for Encephalopathy
Status: Enrolling
Updated:  8/26/2013
University of Utah
703
mi
from 98109
Salt Lake City, UT
Darbe Administration in Newborns Undergoing Cooling for Encephalopathy
Darbe Administration in Newborns Undergoing Cooling for Encephalopathy
Status: Enrolling
Updated: 8/26/2013
University of Utah
703
mi
from 98109
Salt Lake City, UT
Click here to add this to my saved trials
Darbe Administration in Newborns Undergoing Cooling for Encephalopathy
Darbe Administration in Newborns Undergoing Cooling for Encephalopathy
Status: Enrolling
Updated:  8/26/2013
Intermountain Medical Center
706
mi
from 98109
Sandy, UT
Darbe Administration in Newborns Undergoing Cooling for Encephalopathy
Darbe Administration in Newborns Undergoing Cooling for Encephalopathy
Status: Enrolling
Updated: 8/26/2013
Intermountain Medical Center
706
mi
from 98109
Sandy, UT
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Darbe Administration in Newborns Undergoing Cooling for Encephalopathy
Darbe Administration in Newborns Undergoing Cooling for Encephalopathy
Status: Enrolling
Updated:  8/26/2013
Univ of Washington
2
mi
from 98109
Seattle, WA
Darbe Administration in Newborns Undergoing Cooling for Encephalopathy
Darbe Administration in Newborns Undergoing Cooling for Encephalopathy
Status: Enrolling
Updated: 8/26/2013
Univ of Washington
2
mi
from 98109
Seattle, WA
Click here to add this to my saved trials
A Study to Assess the Safety, Tolerability and PK of a Single IV Dose of ETI-204 in Adult Volunteers
Safety, Tolerability, and PK of a Single Intravenous Dose of ETI-204 in Adult Volunteers
Status: Enrolling
Updated:  8/26/2013
Covance Clinical Research Inc.
1675
mi
from 98109
Dallas, TX
A Study to Assess the Safety, Tolerability and PK of a Single IV Dose of ETI-204 in Adult Volunteers
Safety, Tolerability, and PK of a Single Intravenous Dose of ETI-204 in Adult Volunteers
Status: Enrolling
Updated: 8/26/2013
Covance Clinical Research Inc.
1675
mi
from 98109
Dallas, TX
Click here to add this to my saved trials
Study Comparing High-Dose Flu Vaccine to Standard Vaccine in Cancer Patients Less Than 65 Receiving Chemotherapy
A Randomized Pilot Study Comparing High-Dose Influenza Vaccine to Standard-Dose Influenza Vaccine in Adult Oncology Patients Less Than 65 Years Receiving Chemotherapy
Status: Enrolling
Updated:  8/27/2013
Rochester General Hospital
2160
mi
from 98109
Rochester, NY
Study Comparing High-Dose Flu Vaccine to Standard Vaccine in Cancer Patients Less Than 65 Receiving Chemotherapy
A Randomized Pilot Study Comparing High-Dose Influenza Vaccine to Standard-Dose Influenza Vaccine in Adult Oncology Patients Less Than 65 Years Receiving Chemotherapy
Status: Enrolling
Updated: 8/27/2013
Rochester General Hospital
2160
mi
from 98109
Rochester, NY
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Study Comparing High-Dose Flu Vaccine to Standard Vaccine in Cancer Patients Less Than 65 Receiving Chemotherapy
A Randomized Pilot Study Comparing High-Dose Influenza Vaccine to Standard-Dose Influenza Vaccine in Adult Oncology Patients Less Than 65 Years Receiving Chemotherapy
Status: Enrolling
Updated:  8/27/2013
Lipson Cancer Center Linden Oaks Medical Campus
2161
mi
from 98109
Rochester, NY
Study Comparing High-Dose Flu Vaccine to Standard Vaccine in Cancer Patients Less Than 65 Receiving Chemotherapy
A Randomized Pilot Study Comparing High-Dose Influenza Vaccine to Standard-Dose Influenza Vaccine in Adult Oncology Patients Less Than 65 Years Receiving Chemotherapy
Status: Enrolling
Updated: 8/27/2013
Lipson Cancer Center Linden Oaks Medical Campus
2161
mi
from 98109
Rochester, NY
Click here to add this to my saved trials