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
12,214
archived clinical trials in
Women's Studies

Clinical Evaluation of the BD Onclarity™ HPV Assay on the BD Viper™ LT System With Cervical Specimens
Clinical Evaluation of the BD Onclarity™ HPV Assay on the BD Viper™ LT System With Cervical Specimens
Status: Enrolling
Updated:  12/31/1969
mi
from
San Diego, CA
Clinical Evaluation of the BD Onclarity™ HPV Assay on the BD Viper™ LT System With Cervical Specimens
Clinical Evaluation of the BD Onclarity™ HPV Assay on the BD Viper™ LT System With Cervical Specimens
Status: Enrolling
Updated: 12/31/1969
Women's Health Care Research Corp.
mi
from
San Diego, CA
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Clinical Evaluation of the BD Onclarity™ HPV Assay on the BD Viper™ LT System With Cervical Specimens
Clinical Evaluation of the BD Onclarity™ HPV Assay on the BD Viper™ LT System With Cervical Specimens
Status: Enrolling
Updated:  12/31/1969
mi
from
Teterboro, NJ
Clinical Evaluation of the BD Onclarity™ HPV Assay on the BD Viper™ LT System With Cervical Specimens
Clinical Evaluation of the BD Onclarity™ HPV Assay on the BD Viper™ LT System With Cervical Specimens
Status: Enrolling
Updated: 12/31/1969
Q Squared Solutions
mi
from
Teterboro, NJ
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Clinical Evaluation of the BD Onclarity™ HPV Assay on the BD Viper™ LT System With Cervical Specimens
Clinical Evaluation of the BD Onclarity™ HPV Assay on the BD Viper™ LT System With Cervical Specimens
Status: Enrolling
Updated:  12/31/1969
mi
from
Albuquerque, NM
Clinical Evaluation of the BD Onclarity™ HPV Assay on the BD Viper™ LT System With Cervical Specimens
Clinical Evaluation of the BD Onclarity™ HPV Assay on the BD Viper™ LT System With Cervical Specimens
Status: Enrolling
Updated: 12/31/1969
TriCore Reference Laboratory
mi
from
Albuquerque, NM
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Clinical Evaluation of the BD Onclarity™ HPV Assay on the BD Viper™ LT System With Cervical Specimens
Clinical Evaluation of the BD Onclarity™ HPV Assay on the BD Viper™ LT System With Cervical Specimens
Status: Enrolling
Updated:  12/31/1969
mi
from
Englewood, OH
Clinical Evaluation of the BD Onclarity™ HPV Assay on the BD Viper™ LT System With Cervical Specimens
Clinical Evaluation of the BD Onclarity™ HPV Assay on the BD Viper™ LT System With Cervical Specimens
Status: Enrolling
Updated: 12/31/1969
HWC Women's Research Center
mi
from
Englewood, OH
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Clinical Evaluation of the BD Onclarity™ HPV Assay on the BD Viper™ LT System With Cervical Specimens
Clinical Evaluation of the BD Onclarity™ HPV Assay on the BD Viper™ LT System With Cervical Specimens
Status: Enrolling
Updated:  12/31/1969
mi
from
Draper, UT
Clinical Evaluation of the BD Onclarity™ HPV Assay on the BD Viper™ LT System With Cervical Specimens
Clinical Evaluation of the BD Onclarity™ HPV Assay on the BD Viper™ LT System With Cervical Specimens
Status: Enrolling
Updated: 12/31/1969
Physicians Research Options
mi
from
Draper, UT
Click here to add this to my saved trials
Clinical Evaluation of the BD Onclarity™ HPV Assay on the BD Viper™ LT System With Cervical Specimens
Clinical Evaluation of the BD Onclarity™ HPV Assay on the BD Viper™ LT System With Cervical Specimens
Status: Enrolling
Updated:  12/31/1969
mi
from
Earlysville, VA
Clinical Evaluation of the BD Onclarity™ HPV Assay on the BD Viper™ LT System With Cervical Specimens
Clinical Evaluation of the BD Onclarity™ HPV Assay on the BD Viper™ LT System With Cervical Specimens
Status: Enrolling
Updated: 12/31/1969
Research Pathology Associates
mi
from
Earlysville, VA
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Dose Escalation Study of AST-OPC1 in Spinal Cord Injury
A Phase 1/2a Dose Escalation Study of AST-OPC1 in Subjects With Subacute Cervical Spinal Cord Injury
Status: Enrolling
Updated:  12/31/1969
mi
from
Los Angeles, CA
Dose Escalation Study of AST-OPC1 in Spinal Cord Injury
A Phase 1/2a Dose Escalation Study of AST-OPC1 in Subjects With Subacute Cervical Spinal Cord Injury
Status: Enrolling
Updated: 12/31/1969
Rancho Los Amigos/USC
mi
from
Los Angeles, CA
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Dose Escalation Study of AST-OPC1 in Spinal Cord Injury
A Phase 1/2a Dose Escalation Study of AST-OPC1 in Subjects With Subacute Cervical Spinal Cord Injury
Status: Enrolling
Updated:  12/31/1969
mi
from
Atlanta, GA
Dose Escalation Study of AST-OPC1 in Spinal Cord Injury
A Phase 1/2a Dose Escalation Study of AST-OPC1 in Subjects With Subacute Cervical Spinal Cord Injury
Status: Enrolling
Updated: 12/31/1969
Shepherd Center
mi
from
Atlanta, GA
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Dose Escalation Study of AST-OPC1 in Spinal Cord Injury
A Phase 1/2a Dose Escalation Study of AST-OPC1 in Subjects With Subacute Cervical Spinal Cord Injury
Status: Enrolling
Updated:  12/31/1969
mi
from
Chicago, IL
Dose Escalation Study of AST-OPC1 in Spinal Cord Injury
A Phase 1/2a Dose Escalation Study of AST-OPC1 in Subjects With Subacute Cervical Spinal Cord Injury
Status: Enrolling
Updated: 12/31/1969
Rush University Medical Center
mi
from
Chicago, IL
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Dose Escalation Study of AST-OPC1 in Spinal Cord Injury
A Phase 1/2a Dose Escalation Study of AST-OPC1 in Subjects With Subacute Cervical Spinal Cord Injury
Status: Enrolling
Updated:  12/31/1969
mi
from
Indianapolis, IN
Dose Escalation Study of AST-OPC1 in Spinal Cord Injury
A Phase 1/2a Dose Escalation Study of AST-OPC1 in Subjects With Subacute Cervical Spinal Cord Injury
Status: Enrolling
Updated: 12/31/1969
Indiana University
mi
from
Indianapolis, IN
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Dose Escalation Study of AST-OPC1 in Spinal Cord Injury
A Phase 1/2a Dose Escalation Study of AST-OPC1 in Subjects With Subacute Cervical Spinal Cord Injury
Status: Enrolling
Updated:  12/31/1969
mi
from
Milwaukee, WI
Dose Escalation Study of AST-OPC1 in Spinal Cord Injury
A Phase 1/2a Dose Escalation Study of AST-OPC1 in Subjects With Subacute Cervical Spinal Cord Injury
Status: Enrolling
Updated: 12/31/1969
Medical College of Wisconsin
mi
from
Milwaukee, WI
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Dose Escalation Study of AST-OPC1 in Spinal Cord Injury
A Phase 1/2a Dose Escalation Study of AST-OPC1 in Subjects With Subacute Cervical Spinal Cord Injury
Status: Enrolling
Updated:  12/31/1969
mi
from
Saint Louis, MO
Dose Escalation Study of AST-OPC1 in Spinal Cord Injury
A Phase 1/2a Dose Escalation Study of AST-OPC1 in Subjects With Subacute Cervical Spinal Cord Injury
Status: Enrolling
Updated: 12/31/1969
Washington University
mi
from
Saint Louis, MO
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Dose Escalation Study of AST-OPC1 in Spinal Cord Injury
A Phase 1/2a Dose Escalation Study of AST-OPC1 in Subjects With Subacute Cervical Spinal Cord Injury
Status: Enrolling
Updated:  12/31/1969
mi
from
Philadelphia, PA
Dose Escalation Study of AST-OPC1 in Spinal Cord Injury
A Phase 1/2a Dose Escalation Study of AST-OPC1 in Subjects With Subacute Cervical Spinal Cord Injury
Status: Enrolling
Updated: 12/31/1969
Thomas Jefferson University/Magee Rehabilitation
mi
from
Philadelphia, PA
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Dose Escalation Study of AST-OPC1 in Spinal Cord Injury
A Phase 1/2a Dose Escalation Study of AST-OPC1 in Subjects With Subacute Cervical Spinal Cord Injury
Status: Enrolling
Updated:  12/31/1969
mi
from
La Jolla, CA
Dose Escalation Study of AST-OPC1 in Spinal Cord Injury
A Phase 1/2a Dose Escalation Study of AST-OPC1 in Subjects With Subacute Cervical Spinal Cord Injury
Status: Enrolling
Updated: 12/31/1969
The University of California, San Diego
mi
from
La Jolla, CA
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Dose Escalation Study of AST-OPC1 in Spinal Cord Injury
A Phase 1/2a Dose Escalation Study of AST-OPC1 in Subjects With Subacute Cervical Spinal Cord Injury
Status: Enrolling
Updated:  12/31/1969
mi
from
San Jose, CA
Dose Escalation Study of AST-OPC1 in Spinal Cord Injury
A Phase 1/2a Dose Escalation Study of AST-OPC1 in Subjects With Subacute Cervical Spinal Cord Injury
Status: Enrolling
Updated: 12/31/1969
Stanford University/Santa Clara Valley Medical Center
mi
from
San Jose, CA
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Onabotulinumtoxin A Versus Kenalog for Chronic Pelvic Pain
A Double-Blind, Randomized Study to Compare Onabotulinumtoxin A Versus Kenalog for Intravaginal Trigger Point Injections in the Treatment of Chronic Pelvic Pain
Status: Enrolling
Updated:  12/31/1969
mi
from
Royal Oak, MI
Onabotulinumtoxin A Versus Kenalog for Chronic Pelvic Pain
A Double-Blind, Randomized Study to Compare Onabotulinumtoxin A Versus Kenalog for Intravaginal Trigger Point Injections in the Treatment of Chronic Pelvic Pain
Status: Enrolling
Updated: 12/31/1969
Beaumont Hospitals
mi
from
Royal Oak, MI
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RAINBOW Study: RAnibizumab Compared With Laser Therapy for the Treatment of INfants BOrn Prematurely With Retinopathy of Prematurity
RAINBOW Study: a Randomized, Controlled Study Evaluating the Efficacy and Safety of RAnibizumab Compared With Laser Therapy for the Treatment of INfants BOrn Prematurely With Retinopathy of Prematurity
Status: Enrolling
Updated:  12/31/1969
mi
from
Graz,
RAINBOW Study: RAnibizumab Compared With Laser Therapy for the Treatment of INfants BOrn Prematurely With Retinopathy of Prematurity
RAINBOW Study: a Randomized, Controlled Study Evaluating the Efficacy and Safety of RAnibizumab Compared With Laser Therapy for the Treatment of INfants BOrn Prematurely With Retinopathy of Prematurity
Status: Enrolling
Updated: 12/31/1969
Novartis Investigative Site
mi
from
Graz,
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RAINBOW Study: RAnibizumab Compared With Laser Therapy for the Treatment of INfants BOrn Prematurely With Retinopathy of Prematurity
RAINBOW Study: a Randomized, Controlled Study Evaluating the Efficacy and Safety of RAnibizumab Compared With Laser Therapy for the Treatment of INfants BOrn Prematurely With Retinopathy of Prematurity
Status: Enrolling
Updated:  12/31/1969
mi
from
Sacramento, CA
RAINBOW Study: RAnibizumab Compared With Laser Therapy for the Treatment of INfants BOrn Prematurely With Retinopathy of Prematurity
RAINBOW Study: a Randomized, Controlled Study Evaluating the Efficacy and Safety of RAnibizumab Compared With Laser Therapy for the Treatment of INfants BOrn Prematurely With Retinopathy of Prematurity
Status: Enrolling
Updated: 12/31/1969
Novartis Investigative Site
mi
from
Sacramento, CA
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RAINBOW Study: RAnibizumab Compared With Laser Therapy for the Treatment of INfants BOrn Prematurely With Retinopathy of Prematurity
RAINBOW Study: a Randomized, Controlled Study Evaluating the Efficacy and Safety of RAnibizumab Compared With Laser Therapy for the Treatment of INfants BOrn Prematurely With Retinopathy of Prematurity
Status: Enrolling
Updated:  12/31/1969
mi
from
Salt Lake City, UT
RAINBOW Study: RAnibizumab Compared With Laser Therapy for the Treatment of INfants BOrn Prematurely With Retinopathy of Prematurity
RAINBOW Study: a Randomized, Controlled Study Evaluating the Efficacy and Safety of RAnibizumab Compared With Laser Therapy for the Treatment of INfants BOrn Prematurely With Retinopathy of Prematurity
Status: Enrolling
Updated: 12/31/1969
Novartis Investigative Site
mi
from
Salt Lake City, UT
Click here to add this to my saved trials
RAINBOW Study: RAnibizumab Compared With Laser Therapy for the Treatment of INfants BOrn Prematurely With Retinopathy of Prematurity
RAINBOW Study: a Randomized, Controlled Study Evaluating the Efficacy and Safety of RAnibizumab Compared With Laser Therapy for the Treatment of INfants BOrn Prematurely With Retinopathy of Prematurity
Status: Enrolling
Updated:  12/31/1969
mi
from
Loma Linda, CA
RAINBOW Study: RAnibizumab Compared With Laser Therapy for the Treatment of INfants BOrn Prematurely With Retinopathy of Prematurity
RAINBOW Study: a Randomized, Controlled Study Evaluating the Efficacy and Safety of RAnibizumab Compared With Laser Therapy for the Treatment of INfants BOrn Prematurely With Retinopathy of Prematurity
Status: Enrolling
Updated: 12/31/1969
Novartis Investigative Site
mi
from
Loma Linda, CA
Click here to add this to my saved trials
RAINBOW Study: RAnibizumab Compared With Laser Therapy for the Treatment of INfants BOrn Prematurely With Retinopathy of Prematurity
RAINBOW Study: a Randomized, Controlled Study Evaluating the Efficacy and Safety of RAnibizumab Compared With Laser Therapy for the Treatment of INfants BOrn Prematurely With Retinopathy of Prematurity
Status: Enrolling
Updated:  12/31/1969
mi
from
Chicago, IL
RAINBOW Study: RAnibizumab Compared With Laser Therapy for the Treatment of INfants BOrn Prematurely With Retinopathy of Prematurity
RAINBOW Study: a Randomized, Controlled Study Evaluating the Efficacy and Safety of RAnibizumab Compared With Laser Therapy for the Treatment of INfants BOrn Prematurely With Retinopathy of Prematurity
Status: Enrolling
Updated: 12/31/1969
Novartis Investigator Site
mi
from
Chicago, IL
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RAINBOW Study: RAnibizumab Compared With Laser Therapy for the Treatment of INfants BOrn Prematurely With Retinopathy of Prematurity
RAINBOW Study: a Randomized, Controlled Study Evaluating the Efficacy and Safety of RAnibizumab Compared With Laser Therapy for the Treatment of INfants BOrn Prematurely With Retinopathy of Prematurity
Status: Enrolling
Updated:  12/31/1969
mi
from
Louisville, KY
RAINBOW Study: RAnibizumab Compared With Laser Therapy for the Treatment of INfants BOrn Prematurely With Retinopathy of Prematurity
RAINBOW Study: a Randomized, Controlled Study Evaluating the Efficacy and Safety of RAnibizumab Compared With Laser Therapy for the Treatment of INfants BOrn Prematurely With Retinopathy of Prematurity
Status: Enrolling
Updated: 12/31/1969
Novartis Investigative Site
mi
from
Louisville, KY
Click here to add this to my saved trials
RAINBOW Study: RAnibizumab Compared With Laser Therapy for the Treatment of INfants BOrn Prematurely With Retinopathy of Prematurity
RAINBOW Study: a Randomized, Controlled Study Evaluating the Efficacy and Safety of RAnibizumab Compared With Laser Therapy for the Treatment of INfants BOrn Prematurely With Retinopathy of Prematurity
Status: Enrolling
Updated:  12/31/1969
mi
from
Boston, MA
RAINBOW Study: RAnibizumab Compared With Laser Therapy for the Treatment of INfants BOrn Prematurely With Retinopathy of Prematurity
RAINBOW Study: a Randomized, Controlled Study Evaluating the Efficacy and Safety of RAnibizumab Compared With Laser Therapy for the Treatment of INfants BOrn Prematurely With Retinopathy of Prematurity
Status: Enrolling
Updated: 12/31/1969
Novartis Investigative site
mi
from
Boston, MA
Click here to add this to my saved trials
RAINBOW Study: RAnibizumab Compared With Laser Therapy for the Treatment of INfants BOrn Prematurely With Retinopathy of Prematurity
RAINBOW Study: a Randomized, Controlled Study Evaluating the Efficacy and Safety of RAnibizumab Compared With Laser Therapy for the Treatment of INfants BOrn Prematurely With Retinopathy of Prematurity
Status: Enrolling
Updated:  12/31/1969
mi
from
Ann Arbor, MI
RAINBOW Study: RAnibizumab Compared With Laser Therapy for the Treatment of INfants BOrn Prematurely With Retinopathy of Prematurity
RAINBOW Study: a Randomized, Controlled Study Evaluating the Efficacy and Safety of RAnibizumab Compared With Laser Therapy for the Treatment of INfants BOrn Prematurely With Retinopathy of Prematurity
Status: Enrolling
Updated: 12/31/1969
Novartis Investigative Site
mi
from
Ann Arbor, MI
Click here to add this to my saved trials
RAINBOW Study: RAnibizumab Compared With Laser Therapy for the Treatment of INfants BOrn Prematurely With Retinopathy of Prematurity
RAINBOW Study: a Randomized, Controlled Study Evaluating the Efficacy and Safety of RAnibizumab Compared With Laser Therapy for the Treatment of INfants BOrn Prematurely With Retinopathy of Prematurity
Status: Enrolling
Updated:  12/31/1969
mi
from
Rochester, NY
RAINBOW Study: RAnibizumab Compared With Laser Therapy for the Treatment of INfants BOrn Prematurely With Retinopathy of Prematurity
RAINBOW Study: a Randomized, Controlled Study Evaluating the Efficacy and Safety of RAnibizumab Compared With Laser Therapy for the Treatment of INfants BOrn Prematurely With Retinopathy of Prematurity
Status: Enrolling
Updated: 12/31/1969
Novartis Investigative Site
mi
from
Rochester, NY
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RAINBOW Study: RAnibizumab Compared With Laser Therapy for the Treatment of INfants BOrn Prematurely With Retinopathy of Prematurity
RAINBOW Study: a Randomized, Controlled Study Evaluating the Efficacy and Safety of RAnibizumab Compared With Laser Therapy for the Treatment of INfants BOrn Prematurely With Retinopathy of Prematurity
Status: Enrolling
Updated:  12/31/1969
mi
from
Morgantown, WV
RAINBOW Study: RAnibizumab Compared With Laser Therapy for the Treatment of INfants BOrn Prematurely With Retinopathy of Prematurity
RAINBOW Study: a Randomized, Controlled Study Evaluating the Efficacy and Safety of RAnibizumab Compared With Laser Therapy for the Treatment of INfants BOrn Prematurely With Retinopathy of Prematurity
Status: Enrolling
Updated: 12/31/1969
Novartis Investigative Site
mi
from
Morgantown, WV
Click here to add this to my saved trials
RAINBOW Study: RAnibizumab Compared With Laser Therapy for the Treatment of INfants BOrn Prematurely With Retinopathy of Prematurity
RAINBOW Study: a Randomized, Controlled Study Evaluating the Efficacy and Safety of RAnibizumab Compared With Laser Therapy for the Treatment of INfants BOrn Prematurely With Retinopathy of Prematurity
Status: Enrolling
Updated:  12/31/1969
mi
from
Aurora, CO
RAINBOW Study: RAnibizumab Compared With Laser Therapy for the Treatment of INfants BOrn Prematurely With Retinopathy of Prematurity
RAINBOW Study: a Randomized, Controlled Study Evaluating the Efficacy and Safety of RAnibizumab Compared With Laser Therapy for the Treatment of INfants BOrn Prematurely With Retinopathy of Prematurity
Status: Enrolling
Updated: 12/31/1969
Novartis Investigative site
mi
from
Aurora, CO
Click here to add this to my saved trials
RAINBOW Study: RAnibizumab Compared With Laser Therapy for the Treatment of INfants BOrn Prematurely With Retinopathy of Prematurity
RAINBOW Study: a Randomized, Controlled Study Evaluating the Efficacy and Safety of RAnibizumab Compared With Laser Therapy for the Treatment of INfants BOrn Prematurely With Retinopathy of Prematurity
Status: Enrolling
Updated:  12/31/1969
mi
from
Baltimore, MD
RAINBOW Study: RAnibizumab Compared With Laser Therapy for the Treatment of INfants BOrn Prematurely With Retinopathy of Prematurity
RAINBOW Study: a Randomized, Controlled Study Evaluating the Efficacy and Safety of RAnibizumab Compared With Laser Therapy for the Treatment of INfants BOrn Prematurely With Retinopathy of Prematurity
Status: Enrolling
Updated: 12/31/1969
Novartis
mi
from
Baltimore, MD
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RAINBOW Study: RAnibizumab Compared With Laser Therapy for the Treatment of INfants BOrn Prematurely With Retinopathy of Prematurity
RAINBOW Study: a Randomized, Controlled Study Evaluating the Efficacy and Safety of RAnibizumab Compared With Laser Therapy for the Treatment of INfants BOrn Prematurely With Retinopathy of Prematurity
Status: Enrolling
Updated:  12/31/1969
mi
from
Austin, TX
RAINBOW Study: RAnibizumab Compared With Laser Therapy for the Treatment of INfants BOrn Prematurely With Retinopathy of Prematurity
RAINBOW Study: a Randomized, Controlled Study Evaluating the Efficacy and Safety of RAnibizumab Compared With Laser Therapy for the Treatment of INfants BOrn Prematurely With Retinopathy of Prematurity
Status: Enrolling
Updated: 12/31/1969
Novartis Investigational Site
mi
from
Austin, TX
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Apollo™ Onyx™ Delivery Micro Catheter Post Market Safety Study
Apollo™ Onyx™ Delivery Micro Catheter Post Market Safety Study
Status: Enrolling
Updated:  12/31/1969
mi
from
Englewood, CO
Apollo™ Onyx™ Delivery Micro Catheter Post Market Safety Study
Apollo™ Onyx™ Delivery Micro Catheter Post Market Safety Study
Status: Enrolling
Updated: 12/31/1969
Radiology Imaging Associates
mi
from
Englewood, CO
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Apollo™ Onyx™ Delivery Micro Catheter Post Market Safety Study
Apollo™ Onyx™ Delivery Micro Catheter Post Market Safety Study
Status: Enrolling
Updated:  12/31/1969
mi
from
Boston, MA
Apollo™ Onyx™ Delivery Micro Catheter Post Market Safety Study
Apollo™ Onyx™ Delivery Micro Catheter Post Market Safety Study
Status: Enrolling
Updated: 12/31/1969
Brigham's & Women Hospital
mi
from
Boston, MA
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Safety and Efficacy of PNEUMOSTEM® in Premature Infants at High Risk for Bronchopulmonary Dysplasia (BPD) - a US Study
A Phase I/II, Open-Label Dose Escalation Trial to Evaluate the Safety and Efficacy of Two Dose Levels of PNEUMOSTEM® in Premature Infants at High Risk for Bronchopulmonary Dysplasia (BPD)
Status: Enrolling
Updated:  12/31/1969
mi
from
Chicago, IL
Safety and Efficacy of PNEUMOSTEM® in Premature Infants at High Risk for Bronchopulmonary Dysplasia (BPD) - a US Study
A Phase I/II, Open-Label Dose Escalation Trial to Evaluate the Safety and Efficacy of Two Dose Levels of PNEUMOSTEM® in Premature Infants at High Risk for Bronchopulmonary Dysplasia (BPD)
Status: Enrolling
Updated: 12/31/1969
Rush University Medical Center
mi
from
Chicago, IL
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Prospective, Observational Registry of Renaissance-guided Spine Surgeries
Prospective, Observational Registry of Renaissance-guided Spine Surgeries
Status: Enrolling
Updated:  12/31/1969
mi
from
Jacksonville, FL
Prospective, Observational Registry of Renaissance-guided Spine Surgeries
Prospective, Observational Registry of Renaissance-guided Spine Surgeries
Status: Enrolling
Updated: 12/31/1969
Lyerly Baptist/ Lyerly Neurosurgery
mi
from
Jacksonville, FL
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Prospective, Observational Registry of Renaissance-guided Spine Surgeries
Prospective, Observational Registry of Renaissance-guided Spine Surgeries
Status: Enrolling
Updated:  12/31/1969
mi
from
Memphis, TN
Prospective, Observational Registry of Renaissance-guided Spine Surgeries
Prospective, Observational Registry of Renaissance-guided Spine Surgeries
Status: Enrolling
Updated: 12/31/1969
Tabor Orthopedics
mi
from
Memphis, TN
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Prospective, Observational Registry of Renaissance-guided Spine Surgeries
Prospective, Observational Registry of Renaissance-guided Spine Surgeries
Status: Enrolling
Updated:  12/31/1969
mi
from
Houston, TX
Prospective, Observational Registry of Renaissance-guided Spine Surgeries
Prospective, Observational Registry of Renaissance-guided Spine Surgeries
Status: Enrolling
Updated: 12/31/1969
Spine Associates
mi
from
Houston, TX
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Prospective, Observational Registry of Renaissance-guided Spine Surgeries
Prospective, Observational Registry of Renaissance-guided Spine Surgeries
Status: Enrolling
Updated:  12/31/1969
mi
from
Reston, VA
Prospective, Observational Registry of Renaissance-guided Spine Surgeries
Prospective, Observational Registry of Renaissance-guided Spine Surgeries
Status: Enrolling
Updated: 12/31/1969
Virginia Spine Institute
mi
from
Reston, VA
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Transplacental Gradients and Transport in Intrauterine Growth Restricted (IUGR) Pregnancies Compared to Normal Pregnancies.
Project 1A) To Determine Whether the Transplacental Gradients for 6 Polyols and Mannose Are Altered in IUGR Pregnancies Compared to Normal Pregnancies. Project 1B) To Determine the Relative Contributions of Transplacental Transport vs. Production by the Conceptus of Both Myoinositol (Major Polyol) and Mannose in IUGR and Normal Pregnancies Using Stable Isotopic Methodology.
Status: Enrolling
Updated:  12/31/1969
mi
from
Aurora, CO
Transplacental Gradients and Transport in Intrauterine Growth Restricted (IUGR) Pregnancies Compared to Normal Pregnancies.
Project 1A) To Determine Whether the Transplacental Gradients for 6 Polyols and Mannose Are Altered in IUGR Pregnancies Compared to Normal Pregnancies. Project 1B) To Determine the Relative Contributions of Transplacental Transport vs. Production by the Conceptus of Both Myoinositol (Major Polyol) and Mannose in IUGR and Normal Pregnancies Using Stable Isotopic Methodology.
Status: Enrolling
Updated: 12/31/1969
University of Colorado Denver Anschutz Medical Campus
mi
from
Aurora, CO
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Phase II Evaluation of AHCC for the Eradication of HPV Infections
Phase II Randomized, Double-blind, Placebo-controlled Evaluation of AHCC (Active Hexose Correlated Compound) for the Eradication of HPV Infections in Women With HPV Positive Pap Smears
Status: Enrolling
Updated:  12/31/1969
mi
from
Houston, TX
Phase II Evaluation of AHCC for the Eradication of HPV Infections
Phase II Randomized, Double-blind, Placebo-controlled Evaluation of AHCC (Active Hexose Correlated Compound) for the Eradication of HPV Infections in Women With HPV Positive Pap Smears
Status: Enrolling
Updated: 12/31/1969
UTHealth Medical School at Houston
mi
from
Houston, TX
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Use of Contrast Enhanced Spectral Mammography (CESM) for Women With Palpable Breast Abnormalities
Use of Contrast Enhanced Spectral Mammography (CESM) for Women With Palpable Breast Abnormalities
Status: Enrolling
Updated:  12/31/1969
mi
from
New York, NY
Use of Contrast Enhanced Spectral Mammography (CESM) for Women With Palpable Breast Abnormalities
Use of Contrast Enhanced Spectral Mammography (CESM) for Women With Palpable Breast Abnormalities
Status: Enrolling
Updated: 12/31/1969
Memorial Sloan Kettering Cancer Center
mi
from
New York, NY
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Effect of Adjunctive Misoprostol Treatment on Blood Loss at Vaginal Delivery
Effect of Adjunctive Misoprostol on Blood Loss at Vaginal Delivery
Status: Enrolling
Updated:  12/31/1969
mi
from
Jamaica, NY
Effect of Adjunctive Misoprostol Treatment on Blood Loss at Vaginal Delivery
Effect of Adjunctive Misoprostol on Blood Loss at Vaginal Delivery
Status: Enrolling
Updated: 12/31/1969
Queens Hospital Center
mi
from
Jamaica, NY
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Peer-to-Peer Support Program in Improving Quality of Life Outcomes in Patients With Gynecologic Cancer and Their Caregivers
Quality of Life Outcomes From a Peer-to-Peer Support Program for Women With Gynecologic Cancer
Status: Enrolling
Updated:  12/31/1969
mi
from
Duarte, CA
Peer-to-Peer Support Program in Improving Quality of Life Outcomes in Patients With Gynecologic Cancer and Their Caregivers
Quality of Life Outcomes From a Peer-to-Peer Support Program for Women With Gynecologic Cancer
Status: Enrolling
Updated: 12/31/1969
City of Hope Medical Center
mi
from
Duarte, CA
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Safety and Efficacy of Pre-incisional Intravenous Ibuprofen to Reduce Postoperative Pain and Opioid Dependence After Posterior Cervical or Lumbar Instrumented Spine Surgery
Safety and Efficacy of Pre-incisional Intravenous Ibuprofen to Reduce Postoperative Pain and Opioid Dependence After Posterior Cervical or Lumbar Instrumented Spine Surgery
Status: Enrolling
Updated:  12/31/1969
mi
from
Phoenix, AZ
Safety and Efficacy of Pre-incisional Intravenous Ibuprofen to Reduce Postoperative Pain and Opioid Dependence After Posterior Cervical or Lumbar Instrumented Spine Surgery
Safety and Efficacy of Pre-incisional Intravenous Ibuprofen to Reduce Postoperative Pain and Opioid Dependence After Posterior Cervical or Lumbar Instrumented Spine Surgery
Status: Enrolling
Updated: 12/31/1969
SJHMC/Barrow Neurosurgical Associates
mi
from
Phoenix, AZ
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Use of High-Resolution Microendoscopy (HRME) in Patients With Cervical Dysplasia
Use of High-Resolution Microendoscopy (HRME) in Patients With Cervical Dysplasia
Status: Enrolling
Updated:  12/31/1969
mi
from
Houston, TX
Use of High-Resolution Microendoscopy (HRME) in Patients With Cervical Dysplasia
Use of High-Resolution Microendoscopy (HRME) in Patients With Cervical Dysplasia
Status: Enrolling
Updated: 12/31/1969
Lyndon B. Johnson General Hospital
mi
from
Houston, TX
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Use of High-Resolution Microendoscopy (HRME) in Patients With Cervical Dysplasia
Use of High-Resolution Microendoscopy (HRME) in Patients With Cervical Dysplasia
Status: Enrolling
Updated:  12/31/1969
mi
from
Houston, TX
Use of High-Resolution Microendoscopy (HRME) in Patients With Cervical Dysplasia
Use of High-Resolution Microendoscopy (HRME) in Patients With Cervical Dysplasia
Status: Enrolling
Updated: 12/31/1969
University of Texas M.D. Anderson Cancer Center
mi
from
Houston, TX
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The CSF Shunt Entry Site Trial
A Randomized Controlled Trial of Anterior Versus Posterior Entry Site for Cerebrospinal Fluid Shunt Insertion
Status: Enrolling
Updated:  12/31/1969
mi
from
Birmingham, AL
The CSF Shunt Entry Site Trial
A Randomized Controlled Trial of Anterior Versus Posterior Entry Site for Cerebrospinal Fluid Shunt Insertion
Status: Enrolling
Updated: 12/31/1969
Children's Hospital of Alabama
mi
from
Birmingham, AL
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The CSF Shunt Entry Site Trial
A Randomized Controlled Trial of Anterior Versus Posterior Entry Site for Cerebrospinal Fluid Shunt Insertion
Status: Enrolling
Updated:  12/31/1969
mi
from
Pittsburgh, PA
The CSF Shunt Entry Site Trial
A Randomized Controlled Trial of Anterior Versus Posterior Entry Site for Cerebrospinal Fluid Shunt Insertion
Status: Enrolling
Updated: 12/31/1969
Children's Hospital of Pittsburgh
mi
from
Pittsburgh, PA
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The CSF Shunt Entry Site Trial
A Randomized Controlled Trial of Anterior Versus Posterior Entry Site for Cerebrospinal Fluid Shunt Insertion
Status: Enrolling
Updated:  12/31/1969
mi
from
Nashville, TN
The CSF Shunt Entry Site Trial
A Randomized Controlled Trial of Anterior Versus Posterior Entry Site for Cerebrospinal Fluid Shunt Insertion
Status: Enrolling
Updated: 12/31/1969
Monroe Carell Jr. Children's Hospital at Vanderbilt
mi
from
Nashville, TN
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The CSF Shunt Entry Site Trial
A Randomized Controlled Trial of Anterior Versus Posterior Entry Site for Cerebrospinal Fluid Shunt Insertion
Status: Enrolling
Updated:  12/31/1969
mi
from
Houston, TX
The CSF Shunt Entry Site Trial
A Randomized Controlled Trial of Anterior Versus Posterior Entry Site for Cerebrospinal Fluid Shunt Insertion
Status: Enrolling
Updated: 12/31/1969
Texas Children's Hospital
mi
from
Houston, TX
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The CSF Shunt Entry Site Trial
A Randomized Controlled Trial of Anterior Versus Posterior Entry Site for Cerebrospinal Fluid Shunt Insertion
Status: Enrolling
Updated:  12/31/1969
mi
from
Salt Lake City, UT
The CSF Shunt Entry Site Trial
A Randomized Controlled Trial of Anterior Versus Posterior Entry Site for Cerebrospinal Fluid Shunt Insertion
Status: Enrolling
Updated: 12/31/1969
Primary Children's Medical Center
mi
from
Salt Lake City, UT
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The CSF Shunt Entry Site Trial
A Randomized Controlled Trial of Anterior Versus Posterior Entry Site for Cerebrospinal Fluid Shunt Insertion
Status: Enrolling
Updated:  12/31/1969
mi
from
Seattle, WA
The CSF Shunt Entry Site Trial
A Randomized Controlled Trial of Anterior Versus Posterior Entry Site for Cerebrospinal Fluid Shunt Insertion
Status: Enrolling
Updated: 12/31/1969
Seattle Children's Hospital
mi
from
Seattle, WA
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