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
10,154
archived clinical trials in
Other Indications

Coenzyme Q10 in Relieving Treatment-Related Fatigue in Women With Breast Cancer
A Randomized Double-Blind Placebo-Controlled Study Of Oral Coenzyme Q10 To Relieve Self-Reported Cancer Treatment Related Fatigue In Breast Cancer Patients
Status: Enrolling
Updated:  12/31/1969
mi
from
Hendersonville, NC
Coenzyme Q10 in Relieving Treatment-Related Fatigue in Women With Breast Cancer
A Randomized Double-Blind Placebo-Controlled Study Of Oral Coenzyme Q10 To Relieve Self-Reported Cancer Treatment Related Fatigue In Breast Cancer Patients
Status: Enrolling
Updated: 12/31/1969
Pardee Memorial Hospital
mi
from
Hendersonville, NC
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Coenzyme Q10 in Relieving Treatment-Related Fatigue in Women With Breast Cancer
A Randomized Double-Blind Placebo-Controlled Study Of Oral Coenzyme Q10 To Relieve Self-Reported Cancer Treatment Related Fatigue In Breast Cancer Patients
Status: Enrolling
Updated:  12/31/1969
mi
from
High Point, NC
Coenzyme Q10 in Relieving Treatment-Related Fatigue in Women With Breast Cancer
A Randomized Double-Blind Placebo-Controlled Study Of Oral Coenzyme Q10 To Relieve Self-Reported Cancer Treatment Related Fatigue In Breast Cancer Patients
Status: Enrolling
Updated: 12/31/1969
High Point Regional Hospital
mi
from
High Point, NC
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Coenzyme Q10 in Relieving Treatment-Related Fatigue in Women With Breast Cancer
A Randomized Double-Blind Placebo-Controlled Study Of Oral Coenzyme Q10 To Relieve Self-Reported Cancer Treatment Related Fatigue In Breast Cancer Patients
Status: Enrolling
Updated:  12/31/1969
mi
from
Lenoir, NC
Coenzyme Q10 in Relieving Treatment-Related Fatigue in Women With Breast Cancer
A Randomized Double-Blind Placebo-Controlled Study Of Oral Coenzyme Q10 To Relieve Self-Reported Cancer Treatment Related Fatigue In Breast Cancer Patients
Status: Enrolling
Updated: 12/31/1969
Caldwell Memorial Hospital
mi
from
Lenoir, NC
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Coenzyme Q10 in Relieving Treatment-Related Fatigue in Women With Breast Cancer
A Randomized Double-Blind Placebo-Controlled Study Of Oral Coenzyme Q10 To Relieve Self-Reported Cancer Treatment Related Fatigue In Breast Cancer Patients
Status: Enrolling
Updated:  12/31/1969
mi
from
Winston-Salem, NC
Coenzyme Q10 in Relieving Treatment-Related Fatigue in Women With Breast Cancer
A Randomized Double-Blind Placebo-Controlled Study Of Oral Coenzyme Q10 To Relieve Self-Reported Cancer Treatment Related Fatigue In Breast Cancer Patients
Status: Enrolling
Updated: 12/31/1969
CCOP - Southeast Cancer Control Consortium
mi
from
Winston-Salem, NC
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Coenzyme Q10 in Relieving Treatment-Related Fatigue in Women With Breast Cancer
A Randomized Double-Blind Placebo-Controlled Study Of Oral Coenzyme Q10 To Relieve Self-Reported Cancer Treatment Related Fatigue In Breast Cancer Patients
Status: Enrolling
Updated:  12/31/1969
mi
from
Winston-Salem, NC
Coenzyme Q10 in Relieving Treatment-Related Fatigue in Women With Breast Cancer
A Randomized Double-Blind Placebo-Controlled Study Of Oral Coenzyme Q10 To Relieve Self-Reported Cancer Treatment Related Fatigue In Breast Cancer Patients
Status: Enrolling
Updated: 12/31/1969
Wake Forest University Comprehensive Cancer Center
mi
from
Winston-Salem, NC
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Coenzyme Q10 in Relieving Treatment-Related Fatigue in Women With Breast Cancer
A Randomized Double-Blind Placebo-Controlled Study Of Oral Coenzyme Q10 To Relieve Self-Reported Cancer Treatment Related Fatigue In Breast Cancer Patients
Status: Enrolling
Updated:  12/31/1969
mi
from
Columbus, OH
Coenzyme Q10 in Relieving Treatment-Related Fatigue in Women With Breast Cancer
A Randomized Double-Blind Placebo-Controlled Study Of Oral Coenzyme Q10 To Relieve Self-Reported Cancer Treatment Related Fatigue In Breast Cancer Patients
Status: Enrolling
Updated: 12/31/1969
CCOP - Columbus
mi
from
Columbus, OH
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Coenzyme Q10 in Relieving Treatment-Related Fatigue in Women With Breast Cancer
A Randomized Double-Blind Placebo-Controlled Study Of Oral Coenzyme Q10 To Relieve Self-Reported Cancer Treatment Related Fatigue In Breast Cancer Patients
Status: Enrolling
Updated:  12/31/1969
mi
from
Greenville, SC
Coenzyme Q10 in Relieving Treatment-Related Fatigue in Women With Breast Cancer
A Randomized Double-Blind Placebo-Controlled Study Of Oral Coenzyme Q10 To Relieve Self-Reported Cancer Treatment Related Fatigue In Breast Cancer Patients
Status: Enrolling
Updated: 12/31/1969
Cancer Centers of the Carolinas - Eastside
mi
from
Greenville, SC
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Coenzyme Q10 in Relieving Treatment-Related Fatigue in Women With Breast Cancer
A Randomized Double-Blind Placebo-Controlled Study Of Oral Coenzyme Q10 To Relieve Self-Reported Cancer Treatment Related Fatigue In Breast Cancer Patients
Status: Enrolling
Updated:  12/31/1969
mi
from
Hilton Head Island, SC
Coenzyme Q10 in Relieving Treatment-Related Fatigue in Women With Breast Cancer
A Randomized Double-Blind Placebo-Controlled Study Of Oral Coenzyme Q10 To Relieve Self-Reported Cancer Treatment Related Fatigue In Breast Cancer Patients
Status: Enrolling
Updated: 12/31/1969
South Carolina Cancer Specialists, PA at Hilton Head Medical Center
mi
from
Hilton Head Island, SC
Click here to add this to my saved trials
Coenzyme Q10 in Relieving Treatment-Related Fatigue in Women With Breast Cancer
A Randomized Double-Blind Placebo-Controlled Study Of Oral Coenzyme Q10 To Relieve Self-Reported Cancer Treatment Related Fatigue In Breast Cancer Patients
Status: Enrolling
Updated:  12/31/1969
mi
from
Spartanburg, SC
Coenzyme Q10 in Relieving Treatment-Related Fatigue in Women With Breast Cancer
A Randomized Double-Blind Placebo-Controlled Study Of Oral Coenzyme Q10 To Relieve Self-Reported Cancer Treatment Related Fatigue In Breast Cancer Patients
Status: Enrolling
Updated: 12/31/1969
CCOP - Upstate Carolina
mi
from
Spartanburg, SC
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Coenzyme Q10 in Relieving Treatment-Related Fatigue in Women With Breast Cancer
A Randomized Double-Blind Placebo-Controlled Study Of Oral Coenzyme Q10 To Relieve Self-Reported Cancer Treatment Related Fatigue In Breast Cancer Patients
Status: Enrolling
Updated:  12/31/1969
mi
from
Danville, VA
Coenzyme Q10 in Relieving Treatment-Related Fatigue in Women With Breast Cancer
A Randomized Double-Blind Placebo-Controlled Study Of Oral Coenzyme Q10 To Relieve Self-Reported Cancer Treatment Related Fatigue In Breast Cancer Patients
Status: Enrolling
Updated: 12/31/1969
Danville Regional Medical Center
mi
from
Danville, VA
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Coenzyme Q10 in Relieving Treatment-Related Fatigue in Women With Breast Cancer
A Randomized Double-Blind Placebo-Controlled Study Of Oral Coenzyme Q10 To Relieve Self-Reported Cancer Treatment Related Fatigue In Breast Cancer Patients
Status: Enrolling
Updated:  12/31/1969
mi
from
Martinsville, VA
Coenzyme Q10 in Relieving Treatment-Related Fatigue in Women With Breast Cancer
A Randomized Double-Blind Placebo-Controlled Study Of Oral Coenzyme Q10 To Relieve Self-Reported Cancer Treatment Related Fatigue In Breast Cancer Patients
Status: Enrolling
Updated: 12/31/1969
Ravenel Oncology Center at Memorial Hospital of Martinsville and Henry County
mi
from
Martinsville, VA
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A Safety and Efficacy Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
A Randomized, Double-Blind, Vehicle-Controlled, Parallel Arm Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
Status: Enrolling
Updated:  12/31/1969
mi
from
Trumbull, CT
A Safety and Efficacy Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
A Randomized, Double-Blind, Vehicle-Controlled, Parallel Arm Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
Status: Enrolling
Updated: 12/31/1969
New England Research Associates, Llc
mi
from
Trumbull, CT
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A Safety and Efficacy Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
A Randomized, Double-Blind, Vehicle-Controlled, Parallel Arm Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
Status: Enrolling
Updated:  12/31/1969
mi
from
Gainesville, FL
A Safety and Efficacy Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
A Randomized, Double-Blind, Vehicle-Controlled, Parallel Arm Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
Status: Enrolling
Updated: 12/31/1969
University of Florida College of Dentristy
mi
from
Gainesville, FL
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A Safety and Efficacy Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
A Randomized, Double-Blind, Vehicle-Controlled, Parallel Arm Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
Status: Enrolling
Updated:  12/31/1969
mi
from
Indianapolis, IN
A Safety and Efficacy Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
A Randomized, Double-Blind, Vehicle-Controlled, Parallel Arm Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
Status: Enrolling
Updated: 12/31/1969
Indiana School of Dentristy
mi
from
Indianapolis, IN
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A Safety and Efficacy Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
A Randomized, Double-Blind, Vehicle-Controlled, Parallel Arm Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
Status: Enrolling
Updated:  12/31/1969
mi
from
Wheaton, MD
A Safety and Efficacy Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
A Randomized, Double-Blind, Vehicle-Controlled, Parallel Arm Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
Status: Enrolling
Updated: 12/31/1969
The Center for Rheumatology and Bone Research
mi
from
Wheaton, MD
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A Safety and Efficacy Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
A Randomized, Double-Blind, Vehicle-Controlled, Parallel Arm Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
Status: Enrolling
Updated:  12/31/1969
mi
from
Boston, MA
A Safety and Efficacy Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
A Randomized, Double-Blind, Vehicle-Controlled, Parallel Arm Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
Status: Enrolling
Updated: 12/31/1969
Tufts University School of Dental Medicine
mi
from
Boston, MA
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A Safety and Efficacy Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
A Randomized, Double-Blind, Vehicle-Controlled, Parallel Arm Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
Status: Enrolling
Updated:  12/31/1969
mi
from
Mineola, NY
A Safety and Efficacy Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
A Randomized, Double-Blind, Vehicle-Controlled, Parallel Arm Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
Status: Enrolling
Updated: 12/31/1969
Winthrop University Hospital
mi
from
Mineola, NY
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A Safety and Efficacy Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
A Randomized, Double-Blind, Vehicle-Controlled, Parallel Arm Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
Status: Enrolling
Updated:  12/31/1969
mi
from
Rochester, NY
A Safety and Efficacy Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
A Randomized, Double-Blind, Vehicle-Controlled, Parallel Arm Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
Status: Enrolling
Updated: 12/31/1969
AAIR Research Center
mi
from
Rochester, NY
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A Safety and Efficacy Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
A Randomized, Double-Blind, Vehicle-Controlled, Parallel Arm Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
Status: Enrolling
Updated:  12/31/1969
mi
from
Charlotte, NC
A Safety and Efficacy Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
A Randomized, Double-Blind, Vehicle-Controlled, Parallel Arm Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
Status: Enrolling
Updated: 12/31/1969
Carolinas Medical Center
mi
from
Charlotte, NC
Click here to add this to my saved trials
A Safety and Efficacy Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
A Randomized, Double-Blind, Vehicle-Controlled, Parallel Arm Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
Status: Enrolling
Updated:  12/31/1969
mi
from
Oklahoma City, OK
A Safety and Efficacy Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
A Randomized, Double-Blind, Vehicle-Controlled, Parallel Arm Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
Status: Enrolling
Updated: 12/31/1969
Oklahoma University
mi
from
Oklahoma City, OK
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A Safety and Efficacy Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
A Randomized, Double-Blind, Vehicle-Controlled, Parallel Arm Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
Status: Enrolling
Updated:  12/31/1969
mi
from
Duncansville, PA
A Safety and Efficacy Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
A Randomized, Double-Blind, Vehicle-Controlled, Parallel Arm Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
Status: Enrolling
Updated: 12/31/1969
Altoona Center for Clinical Research
mi
from
Duncansville, PA
Click here to add this to my saved trials
A Safety and Efficacy Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
A Randomized, Double-Blind, Vehicle-Controlled, Parallel Arm Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
Status: Enrolling
Updated:  12/31/1969
mi
from
Philadelphia, PA
A Safety and Efficacy Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
A Randomized, Double-Blind, Vehicle-Controlled, Parallel Arm Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
Status: Enrolling
Updated: 12/31/1969
Penn Rheumatology Associates
mi
from
Philadelphia, PA
Click here to add this to my saved trials
A Safety and Efficacy Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
A Randomized, Double-Blind, Vehicle-Controlled, Parallel Arm Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
Status: Enrolling
Updated:  12/31/1969
mi
from
Knoxville, TN
A Safety and Efficacy Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
A Randomized, Double-Blind, Vehicle-Controlled, Parallel Arm Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
Status: Enrolling
Updated: 12/31/1969
Rheumatology Consultants Pllc
mi
from
Knoxville, TN
Click here to add this to my saved trials
A Safety and Efficacy Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
A Randomized, Double-Blind, Vehicle-Controlled, Parallel Arm Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
Status: Enrolling
Updated:  12/31/1969
mi
from
Dallas, TX
A Safety and Efficacy Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
A Randomized, Double-Blind, Vehicle-Controlled, Parallel Arm Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
Status: Enrolling
Updated: 12/31/1969
Arthritis Centers of Texas
mi
from
Dallas, TX
Click here to add this to my saved trials
A Safety and Efficacy Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
A Randomized, Double-Blind, Vehicle-Controlled, Parallel Arm Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
Status: Enrolling
Updated:  12/31/1969
mi
from
San Antonio, TX
A Safety and Efficacy Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
A Randomized, Double-Blind, Vehicle-Controlled, Parallel Arm Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
Status: Enrolling
Updated: 12/31/1969
University of Texas Health Science Center
mi
from
San Antonio, TX
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A Safety and Efficacy Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
A Randomized, Double-Blind, Vehicle-Controlled, Parallel Arm Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
Status: Enrolling
Updated:  12/31/1969
mi
from
Spokane, WA
A Safety and Efficacy Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
A Randomized, Double-Blind, Vehicle-Controlled, Parallel Arm Study of 552-02 in Subjects With Dry Mouth Associated With Sjogren's Syndrome
Status: Enrolling
Updated: 12/31/1969
Arthritis Northwest
mi
from
Spokane, WA
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Evaluation of Anti-biofilm Effects of Ferumoxytol (Feraheme) Using an in Situ Biofilm Demineralization Model
Evaluation of Anti-biofilm Effects of Ferumoxytol (Feraheme) Using an in Situ Biofilm Demineralization Model
Status: Enrolling
Updated:  12/31/1969
mi
from
Indianapolis, IN
Evaluation of Anti-biofilm Effects of Ferumoxytol (Feraheme) Using an in Situ Biofilm Demineralization Model
Evaluation of Anti-biofilm Effects of Ferumoxytol (Feraheme) Using an in Situ Biofilm Demineralization Model
Status: Enrolling
Updated: 12/31/1969
Oral Health Research Institute
mi
from
Indianapolis, IN
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Evaluation of Anti-biofilm Effects of Ferumoxytol (Feraheme) Using an in Situ Biofilm Demineralization Model
Evaluation of Anti-biofilm Effects of Ferumoxytol (Feraheme) Using an in Situ Biofilm Demineralization Model
Status: Enrolling
Updated:  12/31/1969
mi
from
Philadelphia, PA
Evaluation of Anti-biofilm Effects of Ferumoxytol (Feraheme) Using an in Situ Biofilm Demineralization Model
Evaluation of Anti-biofilm Effects of Ferumoxytol (Feraheme) Using an in Situ Biofilm Demineralization Model
Status: Enrolling
Updated: 12/31/1969
University of Pennsylvania School of Dental Medicine
mi
from
Philadelphia, PA
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Phase 2 Trial of TD 6424 (Telavancin) Versus Standard Therapy for Complicated Gram Positive Skin and Skin Structure Infections (Gram Positive cSSSI)
A Phase 2, Randomized, Double-Blind, Multinational Trial of Intravenous Telavancin Versus Standard Therapy for Treatment of Complicated Gram Positive Skin and Skin Structure Infections (Gram Positive cSSSI)
Status: Enrolling
Updated:  12/31/1969
mi
from
Chula Vista, CA
Phase 2 Trial of TD 6424 (Telavancin) Versus Standard Therapy for Complicated Gram Positive Skin and Skin Structure Infections (Gram Positive cSSSI)
A Phase 2, Randomized, Double-Blind, Multinational Trial of Intravenous Telavancin Versus Standard Therapy for Treatment of Complicated Gram Positive Skin and Skin Structure Infections (Gram Positive cSSSI)
Status: Enrolling
Updated: 12/31/1969
eStudy Site, 3450 Bonita Road, Ste 201
mi
from
Chula Vista, CA
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Study of URG101 in Painful Bladder Syndrome and Interstitial Cystitis
URG101 Pharmacodynamic and Safety Study: A Randomized, Double-blind, Placebo-controlled, Multi-center Cross-over Study to Investigate the Pharmacodynamic Profile of URG101 in Subjects With Pelvic Pain of Bladder Origin.
Status: Enrolling
Updated:  12/31/1969
mi
from
Glendora, CA
Study of URG101 in Painful Bladder Syndrome and Interstitial Cystitis
URG101 Pharmacodynamic and Safety Study: A Randomized, Double-blind, Placebo-controlled, Multi-center Cross-over Study to Investigate the Pharmacodynamic Profile of URG101 in Subjects With Pelvic Pain of Bladder Origin.
Status: Enrolling
Updated: 12/31/1969
Citrus Valley Medical Research, Inc.
mi
from
Glendora, CA
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Study of URG101 in Painful Bladder Syndrome and Interstitial Cystitis
URG101 Pharmacodynamic and Safety Study: A Randomized, Double-blind, Placebo-controlled, Multi-center Cross-over Study to Investigate the Pharmacodynamic Profile of URG101 in Subjects With Pelvic Pain of Bladder Origin.
Status: Enrolling
Updated:  12/31/1969
mi
from
San Diego, CA
Study of URG101 in Painful Bladder Syndrome and Interstitial Cystitis
URG101 Pharmacodynamic and Safety Study: A Randomized, Double-blind, Placebo-controlled, Multi-center Cross-over Study to Investigate the Pharmacodynamic Profile of URG101 in Subjects With Pelvic Pain of Bladder Origin.
Status: Enrolling
Updated: 12/31/1969
SD Uro-Research
mi
from
San Diego, CA
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Study of URG101 in Painful Bladder Syndrome and Interstitial Cystitis
URG101 Pharmacodynamic and Safety Study: A Randomized, Double-blind, Placebo-controlled, Multi-center Cross-over Study to Investigate the Pharmacodynamic Profile of URG101 in Subjects With Pelvic Pain of Bladder Origin.
Status: Enrolling
Updated:  12/31/1969
mi
from
San Diego, CA
Study of URG101 in Painful Bladder Syndrome and Interstitial Cystitis
URG101 Pharmacodynamic and Safety Study: A Randomized, Double-blind, Placebo-controlled, Multi-center Cross-over Study to Investigate the Pharmacodynamic Profile of URG101 in Subjects With Pelvic Pain of Bladder Origin.
Status: Enrolling
Updated: 12/31/1969
University of California, San Diego
mi
from
San Diego, CA
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Study of URG101 in Painful Bladder Syndrome and Interstitial Cystitis
URG101 Pharmacodynamic and Safety Study: A Randomized, Double-blind, Placebo-controlled, Multi-center Cross-over Study to Investigate the Pharmacodynamic Profile of URG101 in Subjects With Pelvic Pain of Bladder Origin.
Status: Enrolling
Updated:  12/31/1969
mi
from
San Diego, CA
Study of URG101 in Painful Bladder Syndrome and Interstitial Cystitis
URG101 Pharmacodynamic and Safety Study: A Randomized, Double-blind, Placebo-controlled, Multi-center Cross-over Study to Investigate the Pharmacodynamic Profile of URG101 in Subjects With Pelvic Pain of Bladder Origin.
Status: Enrolling
Updated: 12/31/1969
Scripps Clinic Medical Group
mi
from
San Diego, CA
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Study of URG101 in Painful Bladder Syndrome and Interstitial Cystitis
URG101 Pharmacodynamic and Safety Study: A Randomized, Double-blind, Placebo-controlled, Multi-center Cross-over Study to Investigate the Pharmacodynamic Profile of URG101 in Subjects With Pelvic Pain of Bladder Origin.
Status: Enrolling
Updated:  12/31/1969
mi
from
Cartersville, GA
Study of URG101 in Painful Bladder Syndrome and Interstitial Cystitis
URG101 Pharmacodynamic and Safety Study: A Randomized, Double-blind, Placebo-controlled, Multi-center Cross-over Study to Investigate the Pharmacodynamic Profile of URG101 in Subjects With Pelvic Pain of Bladder Origin.
Status: Enrolling
Updated: 12/31/1969
Georgia Urology
mi
from
Cartersville, GA
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Study of URG101 in Painful Bladder Syndrome and Interstitial Cystitis
URG101 Pharmacodynamic and Safety Study: A Randomized, Double-blind, Placebo-controlled, Multi-center Cross-over Study to Investigate the Pharmacodynamic Profile of URG101 in Subjects With Pelvic Pain of Bladder Origin.
Status: Enrolling
Updated:  12/31/1969
mi
from
San Antonio, TX
Study of URG101 in Painful Bladder Syndrome and Interstitial Cystitis
URG101 Pharmacodynamic and Safety Study: A Randomized, Double-blind, Placebo-controlled, Multi-center Cross-over Study to Investigate the Pharmacodynamic Profile of URG101 in Subjects With Pelvic Pain of Bladder Origin.
Status: Enrolling
Updated: 12/31/1969
Urology San Antonio Research
mi
from
San Antonio, TX
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Kerlix Gauze Study in a Burn Trauma Unit and Its Effect on Healthcare Associated Infections in Burn Patients
Kerlix AMD Gauze Study In A Burn Trauma Unit and Its Effect on Healthcare Associated Infections in Burn Patients
Status: Enrolling
Updated:  12/31/1969
mi
from
Iowa City, IA
Kerlix Gauze Study in a Burn Trauma Unit and Its Effect on Healthcare Associated Infections in Burn Patients
Kerlix AMD Gauze Study In A Burn Trauma Unit and Its Effect on Healthcare Associated Infections in Burn Patients
Status: Enrolling
Updated: 12/31/1969
University of Iowa Hospitals and Clinics
mi
from
Iowa City, IA
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Impact of Meditation on Bothersome Tinnitus
Impact of Meditation on Bothersome Tinnitus
Status: Enrolling
Updated:  12/31/1969
mi
from
Buffalo, NY
Impact of Meditation on Bothersome Tinnitus
Impact of Meditation on Bothersome Tinnitus
Status: Enrolling
Updated: 12/31/1969
University at Buffalo
mi
from
Buffalo, NY
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Irradiated Blood Versus Non Irradiated Blood Transfusions in Craniosynostosis Repair
The Affect of Radiated Versus Non-Irradiated Blood on Extracellular Potassium Levels in Infants Undergoing Craniosynostosis Repair
Status: Enrolling
Updated:  12/31/1969
mi
from
Phoenix, AZ
Irradiated Blood Versus Non Irradiated Blood Transfusions in Craniosynostosis Repair
The Affect of Radiated Versus Non-Irradiated Blood on Extracellular Potassium Levels in Infants Undergoing Craniosynostosis Repair
Status: Enrolling
Updated: 12/31/1969
Phoenix Children's Hospital
mi
from
Phoenix, AZ
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Fatigue and Cancer Treatment(FACT)- an Exercise Intervention
Mitigating Cancer Treatment-Related Fatigue by Exercise
Status: Enrolling
Updated:  12/31/1969
mi
from
Baltimore, MD
Fatigue and Cancer Treatment(FACT)- an Exercise Intervention
Mitigating Cancer Treatment-Related Fatigue by Exercise
Status: Enrolling
Updated: 12/31/1969
Johns Hopkins University School of Nursing
mi
from
Baltimore, MD
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Preventing Early Childhood Obesity, Part 1: Family Spirit Nurture, 3-9 Months
Preventing Early Childhood Obesity, Part 1: Family Spirit Nurture, 3-9 Months
Status: Enrolling
Updated:  12/31/1969
mi
from
Shiprock, NM
Preventing Early Childhood Obesity, Part 1: Family Spirit Nurture, 3-9 Months
Preventing Early Childhood Obesity, Part 1: Family Spirit Nurture, 3-9 Months
Status: Enrolling
Updated: 12/31/1969
Johns Hopkins Center for American Indian Health
mi
from
Shiprock, NM
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Randomized Controlled Trial of a Community Health Worker Program on Hearing Loss (Oyendo Bien)
Oyendo Bien: Reducing Disparities in Access to Hearing Health Care on the U.S.-Mexico Border
Status: Enrolling
Updated:  12/31/1969
mi
from
Nogales, AZ
Randomized Controlled Trial of a Community Health Worker Program on Hearing Loss (Oyendo Bien)
Oyendo Bien: Reducing Disparities in Access to Hearing Health Care on the U.S.-Mexico Border
Status: Enrolling
Updated: 12/31/1969
Mariposa Community Health Center
mi
from
Nogales, AZ
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The Effects of Mindfulness-based Stress Reduction in Interstitial Cystitis Patients
The Effects of Mindfulness-based Stress Reduction on the Urinary Microbiome in Patients With Interstitial Cystitis/Painful Bladder Syndrome
Status: Enrolling
Updated:  12/31/1969
mi
from
Cincinnati, OH
The Effects of Mindfulness-based Stress Reduction in Interstitial Cystitis Patients
The Effects of Mindfulness-based Stress Reduction on the Urinary Microbiome in Patients With Interstitial Cystitis/Painful Bladder Syndrome
Status: Enrolling
Updated: 12/31/1969
TriHealth - Cincinnati Urogynecology Associates
mi
from
Cincinnati, OH
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Enabling Personalized Medicine Through Exome Sequencing in the U.S. Air Force
The MilSeq Project: Enabling Personalized Medicine Through Exome Sequencing in the U.S. Air Force
Status: Enrolling
Updated:  12/31/1969
mi
from
Boston, MA
Enabling Personalized Medicine Through Exome Sequencing in the U.S. Air Force
The MilSeq Project: Enabling Personalized Medicine Through Exome Sequencing in the U.S. Air Force
Status: Enrolling
Updated: 12/31/1969
Brigham and Women's Hosp
mi
from
Boston, MA
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Enabling Personalized Medicine Through Exome Sequencing in the U.S. Air Force
The MilSeq Project: Enabling Personalized Medicine Through Exome Sequencing in the U.S. Air Force
Status: Enrolling
Updated:  12/31/1969
mi
from
Biloxi, MS
Enabling Personalized Medicine Through Exome Sequencing in the U.S. Air Force
The MilSeq Project: Enabling Personalized Medicine Through Exome Sequencing in the U.S. Air Force
Status: Enrolling
Updated: 12/31/1969
Keesler Air Force Base
mi
from
Biloxi, MS
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Enabling Personalized Medicine Through Exome Sequencing in the U.S. Air Force
The MilSeq Project: Enabling Personalized Medicine Through Exome Sequencing in the U.S. Air Force
Status: Enrolling
Updated:  12/31/1969
mi
from
Houston, TX
Enabling Personalized Medicine Through Exome Sequencing in the U.S. Air Force
The MilSeq Project: Enabling Personalized Medicine Through Exome Sequencing in the U.S. Air Force
Status: Enrolling
Updated: 12/31/1969
Baylor College of Medicine
mi
from
Houston, TX
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Enabling Personalized Medicine Through Exome Sequencing in the U.S. Air Force
The MilSeq Project: Enabling Personalized Medicine Through Exome Sequencing in the U.S. Air Force
Status: Enrolling
Updated:  12/31/1969
mi
from
San Antonio, TX
Enabling Personalized Medicine Through Exome Sequencing in the U.S. Air Force
The MilSeq Project: Enabling Personalized Medicine Through Exome Sequencing in the U.S. Air Force
Status: Enrolling
Updated: 12/31/1969
Joint Base San Antonio Lackland Air Force Base - 59th Medical Wing
mi
from
San Antonio, TX
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Safety and Tolerability of HemaMax™ (rHuIL-12) as Radiation Countermeasure
A Phase 1b, Single-Dose, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of HemaMax™ (rHuIL-12) in Healthy Subjects
Status: Enrolling
Updated:  12/31/1969
mi
from
Madison, WI
Safety and Tolerability of HemaMax™ (rHuIL-12) as Radiation Countermeasure
A Phase 1b, Single-Dose, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of HemaMax™ (rHuIL-12) in Healthy Subjects
Status: Enrolling
Updated: 12/31/1969
Covance Clinical Research Unit
mi
from
Madison, WI
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Cochlear Promontory Stimulation for Treatment of Tinnitus
Cochlear Promontory Stimulation for Treatment of Tinnitus: Towards Developing an Implantable Device
Status: Enrolling
Updated:  12/31/1969
mi
from
Rochester, MN
Cochlear Promontory Stimulation for Treatment of Tinnitus
Cochlear Promontory Stimulation for Treatment of Tinnitus: Towards Developing an Implantable Device
Status: Enrolling
Updated: 12/31/1969
Mayo Clinic Rochester
mi
from
Rochester, MN
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Vitamin D Deficiency and Atopic Dermatitis
Treatment Of Vitamin D Deficiency And Effect On Atopic Dermatitis Severity
Status: Enrolling
Updated:  12/31/1969
mi
from
Milwaukee, WI
Vitamin D Deficiency and Atopic Dermatitis
Treatment Of Vitamin D Deficiency And Effect On Atopic Dermatitis Severity
Status: Enrolling
Updated: 12/31/1969
Children's Hospital of Wisconsin
mi
from
Milwaukee, WI
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Evaluation of Safety and Reduction of Ear Pain in Adults With Acute Otitis Media and Reduction of Ear Pain in Adults With Acute Otitis Media
Evaluation of Safety and Reduction of Ear Pain in Adults With Acute Otitis Media
Status: Enrolling
Updated:  12/31/1969
mi
from
Bellflower, CA
Evaluation of Safety and Reduction of Ear Pain in Adults With Acute Otitis Media and Reduction of Ear Pain in Adults With Acute Otitis Media
Evaluation of Safety and Reduction of Ear Pain in Adults With Acute Otitis Media
Status: Enrolling
Updated: 12/31/1969
US Clinical Research Group, LLC.
mi
from
Bellflower, CA
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