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

Sustained Aeration of Infant Lungs Trial
Sustained Aeration of Infant Lungs Trial
Status: Enrolling
Updated:  12/31/1969
University of Michigan
mi
from
Ann Arbor, MI
Sustained Aeration of Infant Lungs Trial
Sustained Aeration of Infant Lungs Trial
Status: Enrolling
Updated: 12/31/1969
University of Michigan
mi
from
Ann Arbor, MI
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Sustained Aeration of Infant Lungs Trial
Sustained Aeration of Infant Lungs Trial
Status: Enrolling
Updated:  12/31/1969
Hospital of the Univerity of Pennsylvania
mi
from
Philadelphia, PA
Sustained Aeration of Infant Lungs Trial
Sustained Aeration of Infant Lungs Trial
Status: Enrolling
Updated: 12/31/1969
Hospital of the Univerity of Pennsylvania
mi
from
Philadelphia, PA
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Sustained Aeration of Infant Lungs Trial
Sustained Aeration of Infant Lungs Trial
Status: Enrolling
Updated:  12/31/1969
Pennsylvania Hospital
mi
from
Philadelphia, PA
Sustained Aeration of Infant Lungs Trial
Sustained Aeration of Infant Lungs Trial
Status: Enrolling
Updated: 12/31/1969
Pennsylvania Hospital
mi
from
Philadelphia, PA
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Sustained Aeration of Infant Lungs Trial
Sustained Aeration of Infant Lungs Trial
Status: Enrolling
Updated:  12/31/1969
Women and Infants Hospital of Rhode Island
mi
from
Providence, RI
Sustained Aeration of Infant Lungs Trial
Sustained Aeration of Infant Lungs Trial
Status: Enrolling
Updated: 12/31/1969
Women and Infants Hospital of Rhode Island
mi
from
Providence, RI
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Sustained Aeration of Infant Lungs Trial
Sustained Aeration of Infant Lungs Trial
Status: Enrolling
Updated:  12/31/1969
Loma Linda University
mi
from
Loma Linda, CA
Sustained Aeration of Infant Lungs Trial
Sustained Aeration of Infant Lungs Trial
Status: Enrolling
Updated: 12/31/1969
Loma Linda University
mi
from
Loma Linda, CA
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Sustained Aeration of Infant Lungs Trial
Sustained Aeration of Infant Lungs Trial
Status: Enrolling
Updated:  12/31/1969
Christiana Care
mi
from
Newark, DE
Sustained Aeration of Infant Lungs Trial
Sustained Aeration of Infant Lungs Trial
Status: Enrolling
Updated: 12/31/1969
Christiana Care
mi
from
Newark, DE
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Sustained Aeration of Infant Lungs Trial
Sustained Aeration of Infant Lungs Trial
Status: Enrolling
Updated:  12/31/1969
Wake Med Health
mi
from
Raleigh, NC
Sustained Aeration of Infant Lungs Trial
Sustained Aeration of Infant Lungs Trial
Status: Enrolling
Updated: 12/31/1969
Wake Med Health
mi
from
Raleigh, NC
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Sustained Aeration of Infant Lungs Trial
Sustained Aeration of Infant Lungs Trial
Status: Enrolling
Updated:  12/31/1969
Mater Mother's Hospital
mi
from
Brisbane,
Sustained Aeration of Infant Lungs Trial
Sustained Aeration of Infant Lungs Trial
Status: Enrolling
Updated: 12/31/1969
Mater Mother's Hospital
mi
from
Brisbane,
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Choline Magnesium Trisalicylate and Combination Chemotherapy in Treating Patients With Acute Myeloid Leukemia
A Randomized Phase II Study of Nuclear Factor-kappa B (NF-κB) Inhibition During Induction Chemotherapy for Patients With Acute Myelogenous Leukemia
Status: Enrolling
Updated:  12/31/1969
Rutgers Cancer Institute of New Jersey
mi
from
New Brunswick, NJ
Choline Magnesium Trisalicylate and Combination Chemotherapy in Treating Patients With Acute Myeloid Leukemia
A Randomized Phase II Study of Nuclear Factor-kappa B (NF-κB) Inhibition During Induction Chemotherapy for Patients With Acute Myelogenous Leukemia
Status: Enrolling
Updated: 12/31/1969
Rutgers Cancer Institute of New Jersey
mi
from
New Brunswick, NJ
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Ovarian Morphology and Theca Cell Androgen Production in Women With Polycystic Ovary Syndrome (PCOS)
Ovarian Morphology and Theca Cell Androgen Production in Women With Polycystic Ovary Syndrome (PCOS)
Status: Enrolling
Updated:  12/31/1969
The University of California, San Diego
mi
from
La Jolla, CA
Ovarian Morphology and Theca Cell Androgen Production in Women With Polycystic Ovary Syndrome (PCOS)
Ovarian Morphology and Theca Cell Androgen Production in Women With Polycystic Ovary Syndrome (PCOS)
Status: Enrolling
Updated: 12/31/1969
The University of California, San Diego
mi
from
La Jolla, CA
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A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
A Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
Status: Enrolling
Updated:  12/31/1969
Watson Investigational Site
mi
from
Tucson, AZ
A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
A Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
Status: Enrolling
Updated: 12/31/1969
Watson Investigational Site
mi
from
Tucson, AZ
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A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
A Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
Status: Enrolling
Updated:  12/31/1969
Watson Investigational Site
mi
from
Denver, CO
A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
A Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
Status: Enrolling
Updated: 12/31/1969
Watson Investigational Site
mi
from
Denver, CO
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A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
A Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
Status: Enrolling
Updated:  12/31/1969
Watson Investigational Site
mi
from
Lakewood, CO
A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
A Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
Status: Enrolling
Updated: 12/31/1969
Watson Investigational Site
mi
from
Lakewood, CO
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A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
A Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
Status: Enrolling
Updated:  12/31/1969
Watson Investigational Site
mi
from
Washington,
A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
A Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
Status: Enrolling
Updated: 12/31/1969
Watson Investigational Site
mi
from
Washington,
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A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
A Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
Status: Enrolling
Updated:  12/31/1969
Watson Investigational Site
mi
from
Clearwater, FL
A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
A Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
Status: Enrolling
Updated: 12/31/1969
Watson Investigational Site
mi
from
Clearwater, FL
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A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
A Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
Status: Enrolling
Updated:  12/31/1969
Watson Investigational Site
mi
from
Lake Worth, FL
A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
A Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
Status: Enrolling
Updated: 12/31/1969
Watson Investigational Site
mi
from
Lake Worth, FL
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A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
A Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
Status: Enrolling
Updated:  12/31/1969
Watson Investigational Site
mi
from
Miami, FL
A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
A Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
Status: Enrolling
Updated: 12/31/1969
Watson Investigational Site
mi
from
Miami, FL
Click here to add this to my saved trials
A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
A Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
Status: Enrolling
Updated:  12/31/1969
Watson Investigational Site
mi
from
New Port Richey, FL
A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
A Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
Status: Enrolling
Updated: 12/31/1969
Watson Investigational Site
mi
from
New Port Richey, FL
Click here to add this to my saved trials
A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
A Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
Status: Enrolling
Updated:  12/31/1969
Watson Investigational Site
mi
from
Orlando, FL
A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
A Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
Status: Enrolling
Updated: 12/31/1969
Watson Investigational Site
mi
from
Orlando, FL
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A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
A Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
Status: Enrolling
Updated:  12/31/1969
Watson Investigational Site
mi
from
Atlanta, GA
A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
A Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
Status: Enrolling
Updated: 12/31/1969
Watson Investigational Site
mi
from
Atlanta, GA
Click here to add this to my saved trials
A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
A Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
Status: Enrolling
Updated:  12/31/1969
Watson Investigational Site
mi
from
Atlanta, GA
A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
A Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
Status: Enrolling
Updated: 12/31/1969
Watson Investigational Site
mi
from
Atlanta, GA
Click here to add this to my saved trials
A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
A Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
Status: Enrolling
Updated:  12/31/1969
Watson Investigational Site 111
mi
from
Augusta, GA
A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
A Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
Status: Enrolling
Updated: 12/31/1969
Watson Investigational Site 111
mi
from
Augusta, GA
Click here to add this to my saved trials
A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
A Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
Status: Enrolling
Updated:  12/31/1969
Watson Investigational Site
mi
from
Idaho Falls, ID
A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
A Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
Status: Enrolling
Updated: 12/31/1969
Watson Investigational Site
mi
from
Idaho Falls, ID
Click here to add this to my saved trials
A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
A Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
Status: Enrolling
Updated:  12/31/1969
Watson Investigational Site
mi
from
Brownsburg, IN
A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
A Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
Status: Enrolling
Updated: 12/31/1969
Watson Investigational Site
mi
from
Brownsburg, IN
Click here to add this to my saved trials
A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
A Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
Status: Enrolling
Updated:  12/31/1969
Watson Investigational Site
mi
from
Metairie, LA
A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
A Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
Status: Enrolling
Updated: 12/31/1969
Watson Investigational Site
mi
from
Metairie, LA
Click here to add this to my saved trials
A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
A Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
Status: Enrolling
Updated:  12/31/1969
Watson Investigational Site
mi
from
Norfolk, NE
A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
A Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
Status: Enrolling
Updated: 12/31/1969
Watson Investigational Site
mi
from
Norfolk, NE
Click here to add this to my saved trials
A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
A Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
Status: Enrolling
Updated:  12/31/1969
Watson Investigational Site
mi
from
Albuquerque, NM
A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
A Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
Status: Enrolling
Updated: 12/31/1969
Watson Investigational Site
mi
from
Albuquerque, NM
Click here to add this to my saved trials
A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
A Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
Status: Enrolling
Updated:  12/31/1969
Watson Investigational Site
mi
from
Raleigh, NC
A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
A Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
Status: Enrolling
Updated: 12/31/1969
Watson Investigational Site
mi
from
Raleigh, NC
Click here to add this to my saved trials
A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
A Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
Status: Enrolling
Updated:  12/31/1969
Watson Investigational Site
mi
from
Columbus, OH
A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
A Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
Status: Enrolling
Updated: 12/31/1969
Watson Investigational Site
mi
from
Columbus, OH
Click here to add this to my saved trials
A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
A Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
Status: Enrolling
Updated:  12/31/1969
Watson Investigational Site
mi
from
Jenkintown, PA
A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
A Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
Status: Enrolling
Updated: 12/31/1969
Watson Investigational Site
mi
from
Jenkintown, PA
Click here to add this to my saved trials
A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
A Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
Status: Enrolling
Updated:  12/31/1969
Watson Investigational Site
mi
from
Myrtle Beach, SC
A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
A Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
Status: Enrolling
Updated: 12/31/1969
Watson Investigational Site
mi
from
Myrtle Beach, SC
Click here to add this to my saved trials
A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
A Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
Status: Enrolling
Updated:  12/31/1969
Watson Investigational Site
mi
from
Chattanooga, TN
A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
A Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
Status: Enrolling
Updated: 12/31/1969
Watson Investigational Site
mi
from
Chattanooga, TN
Click here to add this to my saved trials
A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
A Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
Status: Enrolling
Updated:  12/31/1969
Watson Investigational Site
mi
from
Memphis, TN
A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
A Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
Status: Enrolling
Updated: 12/31/1969
Watson Investigational Site
mi
from
Memphis, TN
Click here to add this to my saved trials
A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
A Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
Status: Enrolling
Updated:  12/31/1969
Watson Investigational Site
mi
from
San Diego, CA
A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
A Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
Status: Enrolling
Updated: 12/31/1969
Watson Investigational Site
mi
from
San Diego, CA
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A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
A Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
Status: Enrolling
Updated:  12/31/1969
Watson Investigational Site 116
mi
from
Milford, CT
A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
A Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
Status: Enrolling
Updated: 12/31/1969
Watson Investigational Site 116
mi
from
Milford, CT
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A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
A Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
Status: Enrolling
Updated:  12/31/1969
Watson Investigational Site 129
mi
from
Shawnee Mission, KA
A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
A Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
Status: Enrolling
Updated: 12/31/1969
Watson Investigational Site 129
mi
from
Shawnee Mission, KA
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A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
A Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
Status: Enrolling
Updated:  12/31/1969
Watson Investigational Site
mi
from
Winston-Salem, NC
A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
A Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas
Status: Enrolling
Updated: 12/31/1969
Watson Investigational Site
mi
from
Winston-Salem, NC
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T Cell Receptor Immunotherapy Targeting MAGE-A3 for Patients With Metastatic Cancer Who Are HLA-A*01 Positive
A Phase I-II Study of the Treatment of Metastatic Cancer That Expresses MAGE-A3 Using Lymphodepleting Conditioning Followed by Infusion of Anti-MAGE-A3 HLA-A*01 Restricted TCR-Gene Engineered Lymphocytes and Aldesleukin
Status: Enrolling
Updated:  12/31/1969
National Institutes of Health Clinical Center, 9000 Rockville Pike
mi
from
Bethesda, MD
T Cell Receptor Immunotherapy Targeting MAGE-A3 for Patients With Metastatic Cancer Who Are HLA-A*01 Positive
A Phase I-II Study of the Treatment of Metastatic Cancer That Expresses MAGE-A3 Using Lymphodepleting Conditioning Followed by Infusion of Anti-MAGE-A3 HLA-A*01 Restricted TCR-Gene Engineered Lymphocytes and Aldesleukin
Status: Enrolling
Updated: 12/31/1969
National Institutes of Health Clinical Center, 9000 Rockville Pike
mi
from
Bethesda, MD
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IV Acetaminophen for Postoperative Pain After Pelvic Organ Prolapse Repair
The Impact of IV Acetaminophen on Postoperative Pain in Women Undergoing Pelvic Organ Prolapse Repair: A Double-Blind Randomized Placebo Controlled Trial
Status: Enrolling
Updated:  12/31/1969
Magee-Womens Hospital - University of Pittsburgh Medical Center
mi
from
Pittsburgh, PA
IV Acetaminophen for Postoperative Pain After Pelvic Organ Prolapse Repair
The Impact of IV Acetaminophen on Postoperative Pain in Women Undergoing Pelvic Organ Prolapse Repair: A Double-Blind Randomized Placebo Controlled Trial
Status: Enrolling
Updated: 12/31/1969
Magee-Womens Hospital - University of Pittsburgh Medical Center
mi
from
Pittsburgh, PA
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Connecting Healthy Women: Examining the Effect of an Intervention From the Effect of Being Reachable
Connecting Healthy Women: Examining the Effect of an Intervention From the Effect of Being Reachable
Status: Enrolling
Updated:  12/31/1969
University of Arizona
mi
from
Tucson, AZ
Connecting Healthy Women: Examining the Effect of an Intervention From the Effect of Being Reachable
Connecting Healthy Women: Examining the Effect of an Intervention From the Effect of Being Reachable
Status: Enrolling
Updated: 12/31/1969
University of Arizona
mi
from
Tucson, AZ
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Optimizing Dose of Bupivacaine in Combined Spinal Epidurals To Reduce Side Effects
Randomized Double-blinded Study Designed to Optimize the Dose of Bupivacaine in Combined Spinal Epidurals to Reduce the Incidence of Fetal Bradycardia and Maternal Hypotension
Status: Enrolling
Updated:  12/31/1969
Roosevelt Hospital
mi
from
New York, NY
Optimizing Dose of Bupivacaine in Combined Spinal Epidurals To Reduce Side Effects
Randomized Double-blinded Study Designed to Optimize the Dose of Bupivacaine in Combined Spinal Epidurals to Reduce the Incidence of Fetal Bradycardia and Maternal Hypotension
Status: Enrolling
Updated: 12/31/1969
Roosevelt Hospital
mi
from
New York, NY
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Incubator Weaning of Moderately Preterm Infants
Incubator Weaning of Moderately Preterm Infants: A Randomized Controlled Trial
Status: Enrolling
Updated:  12/31/1969
University of Alabama at Birmingham
mi
from
Birmingham, AL
Incubator Weaning of Moderately Preterm Infants
Incubator Weaning of Moderately Preterm Infants: A Randomized Controlled Trial
Status: Enrolling
Updated: 12/31/1969
University of Alabama at Birmingham
mi
from
Birmingham, AL
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Incubator Weaning of Moderately Preterm Infants
Incubator Weaning of Moderately Preterm Infants: A Randomized Controlled Trial
Status: Enrolling
Updated:  12/31/1969
University of California at Los Angeles
mi
from
Los Angeles, CA
Incubator Weaning of Moderately Preterm Infants
Incubator Weaning of Moderately Preterm Infants: A Randomized Controlled Trial
Status: Enrolling
Updated: 12/31/1969
University of California at Los Angeles
mi
from
Los Angeles, CA
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Incubator Weaning of Moderately Preterm Infants
Incubator Weaning of Moderately Preterm Infants: A Randomized Controlled Trial
Status: Enrolling
Updated:  12/31/1969
Stanford University
mi
from
Palo Alto, CA
Incubator Weaning of Moderately Preterm Infants
Incubator Weaning of Moderately Preterm Infants: A Randomized Controlled Trial
Status: Enrolling
Updated: 12/31/1969
Stanford University
mi
from
Palo Alto, CA
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Incubator Weaning of Moderately Preterm Infants
Incubator Weaning of Moderately Preterm Infants: A Randomized Controlled Trial
Status: Enrolling
Updated:  12/31/1969
Emory University
mi
from
Atlanta, GA
Incubator Weaning of Moderately Preterm Infants
Incubator Weaning of Moderately Preterm Infants: A Randomized Controlled Trial
Status: Enrolling
Updated: 12/31/1969
Emory University
mi
from
Atlanta, GA
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Incubator Weaning of Moderately Preterm Infants
Incubator Weaning of Moderately Preterm Infants: A Randomized Controlled Trial
Status: Enrolling
Updated:  12/31/1969
Indiana University
mi
from
Indianapolis, IN
Incubator Weaning of Moderately Preterm Infants
Incubator Weaning of Moderately Preterm Infants: A Randomized Controlled Trial
Status: Enrolling
Updated: 12/31/1969
Indiana University
mi
from
Indianapolis, IN
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Incubator Weaning of Moderately Preterm Infants
Incubator Weaning of Moderately Preterm Infants: A Randomized Controlled Trial
Status: Enrolling
Updated:  12/31/1969
University of Iowa
mi
from
Iowa City, IA
Incubator Weaning of Moderately Preterm Infants
Incubator Weaning of Moderately Preterm Infants: A Randomized Controlled Trial
Status: Enrolling
Updated: 12/31/1969
University of Iowa
mi
from
Iowa City, IA
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Incubator Weaning of Moderately Preterm Infants
Incubator Weaning of Moderately Preterm Infants: A Randomized Controlled Trial
Status: Enrolling
Updated:  12/31/1969
Wayne State University
mi
from
Detroit, MI
Incubator Weaning of Moderately Preterm Infants
Incubator Weaning of Moderately Preterm Infants: A Randomized Controlled Trial
Status: Enrolling
Updated: 12/31/1969
Wayne State University
mi
from
Detroit, MI
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Incubator Weaning of Moderately Preterm Infants
Incubator Weaning of Moderately Preterm Infants: A Randomized Controlled Trial
Status: Enrolling
Updated:  12/31/1969
Children's Mercy Hospital
mi
from
Kansas City, MO
Incubator Weaning of Moderately Preterm Infants
Incubator Weaning of Moderately Preterm Infants: A Randomized Controlled Trial
Status: Enrolling
Updated: 12/31/1969
Children's Mercy Hospital
mi
from
Kansas City, MO
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Incubator Weaning of Moderately Preterm Infants
Incubator Weaning of Moderately Preterm Infants: A Randomized Controlled Trial
Status: Enrolling
Updated:  12/31/1969
University of New Mexico
mi
from
Albuquerque, NM
Incubator Weaning of Moderately Preterm Infants
Incubator Weaning of Moderately Preterm Infants: A Randomized Controlled Trial
Status: Enrolling
Updated: 12/31/1969
University of New Mexico
mi
from
Albuquerque, NM
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