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
821
archived clinical trials in
Contraception

Study to Evaluate the Contraceptive Efficacy/Safety of a Low Dose EE/LNG Transdermal Contraceptive Delivery System
Open-label, Randomized, Parallel Group, Study of Efficacy and Safety of a Transdermal Contraceptive Delivery System (TCDS) in Comparison to a Low-dose Oral Contraceptive Containing 0.02 mg EE and 0.1 mg LNG in a 21-day Regimen.
Status: Enrolling
Updated:  12/31/1969
Agile Investigational Site
mi
from
Jackson, TN
Study to Evaluate the Contraceptive Efficacy/Safety of a Low Dose EE/LNG Transdermal Contraceptive Delivery System
Open-label, Randomized, Parallel Group, Study of Efficacy and Safety of a Transdermal Contraceptive Delivery System (TCDS) in Comparison to a Low-dose Oral Contraceptive Containing 0.02 mg EE and 0.1 mg LNG in a 21-day Regimen.
Status: Enrolling
Updated: 12/31/1969
Agile Investigational Site
mi
from
Jackson, TN
Click here to add this to my saved trials
Study to Evaluate the Contraceptive Efficacy/Safety of a Low Dose EE/LNG Transdermal Contraceptive Delivery System
Open-label, Randomized, Parallel Group, Study of Efficacy and Safety of a Transdermal Contraceptive Delivery System (TCDS) in Comparison to a Low-dose Oral Contraceptive Containing 0.02 mg EE and 0.1 mg LNG in a 21-day Regimen.
Status: Enrolling
Updated:  12/31/1969
Agile Investigational Site
mi
from
Knoxville, TN
Study to Evaluate the Contraceptive Efficacy/Safety of a Low Dose EE/LNG Transdermal Contraceptive Delivery System
Open-label, Randomized, Parallel Group, Study of Efficacy and Safety of a Transdermal Contraceptive Delivery System (TCDS) in Comparison to a Low-dose Oral Contraceptive Containing 0.02 mg EE and 0.1 mg LNG in a 21-day Regimen.
Status: Enrolling
Updated: 12/31/1969
Agile Investigational Site
mi
from
Knoxville, TN
Click here to add this to my saved trials
Study to Evaluate the Contraceptive Efficacy/Safety of a Low Dose EE/LNG Transdermal Contraceptive Delivery System
Open-label, Randomized, Parallel Group, Study of Efficacy and Safety of a Transdermal Contraceptive Delivery System (TCDS) in Comparison to a Low-dose Oral Contraceptive Containing 0.02 mg EE and 0.1 mg LNG in a 21-day Regimen.
Status: Enrolling
Updated:  12/31/1969
Agile Investigational Site
mi
from
Memphis, TN
Study to Evaluate the Contraceptive Efficacy/Safety of a Low Dose EE/LNG Transdermal Contraceptive Delivery System
Open-label, Randomized, Parallel Group, Study of Efficacy and Safety of a Transdermal Contraceptive Delivery System (TCDS) in Comparison to a Low-dose Oral Contraceptive Containing 0.02 mg EE and 0.1 mg LNG in a 21-day Regimen.
Status: Enrolling
Updated: 12/31/1969
Agile Investigational Site
mi
from
Memphis, TN
Click here to add this to my saved trials
Study to Evaluate the Contraceptive Efficacy/Safety of a Low Dose EE/LNG Transdermal Contraceptive Delivery System
Open-label, Randomized, Parallel Group, Study of Efficacy and Safety of a Transdermal Contraceptive Delivery System (TCDS) in Comparison to a Low-dose Oral Contraceptive Containing 0.02 mg EE and 0.1 mg LNG in a 21-day Regimen.
Status: Enrolling
Updated:  12/31/1969
Agile Investigational Site
mi
from
Austin, TX
Study to Evaluate the Contraceptive Efficacy/Safety of a Low Dose EE/LNG Transdermal Contraceptive Delivery System
Open-label, Randomized, Parallel Group, Study of Efficacy and Safety of a Transdermal Contraceptive Delivery System (TCDS) in Comparison to a Low-dose Oral Contraceptive Containing 0.02 mg EE and 0.1 mg LNG in a 21-day Regimen.
Status: Enrolling
Updated: 12/31/1969
Agile Investigational Site
mi
from
Austin, TX
Click here to add this to my saved trials
Study to Evaluate the Contraceptive Efficacy/Safety of a Low Dose EE/LNG Transdermal Contraceptive Delivery System
Open-label, Randomized, Parallel Group, Study of Efficacy and Safety of a Transdermal Contraceptive Delivery System (TCDS) in Comparison to a Low-dose Oral Contraceptive Containing 0.02 mg EE and 0.1 mg LNG in a 21-day Regimen.
Status: Enrolling
Updated:  12/31/1969
Agile Investigational Site
mi
from
Bedford, TX
Study to Evaluate the Contraceptive Efficacy/Safety of a Low Dose EE/LNG Transdermal Contraceptive Delivery System
Open-label, Randomized, Parallel Group, Study of Efficacy and Safety of a Transdermal Contraceptive Delivery System (TCDS) in Comparison to a Low-dose Oral Contraceptive Containing 0.02 mg EE and 0.1 mg LNG in a 21-day Regimen.
Status: Enrolling
Updated: 12/31/1969
Agile Investigational Site
mi
from
Bedford, TX
Click here to add this to my saved trials
Study to Evaluate the Contraceptive Efficacy/Safety of a Low Dose EE/LNG Transdermal Contraceptive Delivery System
Open-label, Randomized, Parallel Group, Study of Efficacy and Safety of a Transdermal Contraceptive Delivery System (TCDS) in Comparison to a Low-dose Oral Contraceptive Containing 0.02 mg EE and 0.1 mg LNG in a 21-day Regimen.
Status: Enrolling
Updated:  12/31/1969
Agile Investigational Site
mi
from
Corpus Christi, TX
Study to Evaluate the Contraceptive Efficacy/Safety of a Low Dose EE/LNG Transdermal Contraceptive Delivery System
Open-label, Randomized, Parallel Group, Study of Efficacy and Safety of a Transdermal Contraceptive Delivery System (TCDS) in Comparison to a Low-dose Oral Contraceptive Containing 0.02 mg EE and 0.1 mg LNG in a 21-day Regimen.
Status: Enrolling
Updated: 12/31/1969
Agile Investigational Site
mi
from
Corpus Christi, TX
Click here to add this to my saved trials
Study to Evaluate the Contraceptive Efficacy/Safety of a Low Dose EE/LNG Transdermal Contraceptive Delivery System
Open-label, Randomized, Parallel Group, Study of Efficacy and Safety of a Transdermal Contraceptive Delivery System (TCDS) in Comparison to a Low-dose Oral Contraceptive Containing 0.02 mg EE and 0.1 mg LNG in a 21-day Regimen.
Status: Enrolling
Updated:  12/31/1969
Agile Investigational Site
mi
from
Dallas, TX
Study to Evaluate the Contraceptive Efficacy/Safety of a Low Dose EE/LNG Transdermal Contraceptive Delivery System
Open-label, Randomized, Parallel Group, Study of Efficacy and Safety of a Transdermal Contraceptive Delivery System (TCDS) in Comparison to a Low-dose Oral Contraceptive Containing 0.02 mg EE and 0.1 mg LNG in a 21-day Regimen.
Status: Enrolling
Updated: 12/31/1969
Agile Investigational Site
mi
from
Dallas, TX
Click here to add this to my saved trials
Study to Evaluate the Contraceptive Efficacy/Safety of a Low Dose EE/LNG Transdermal Contraceptive Delivery System
Open-label, Randomized, Parallel Group, Study of Efficacy and Safety of a Transdermal Contraceptive Delivery System (TCDS) in Comparison to a Low-dose Oral Contraceptive Containing 0.02 mg EE and 0.1 mg LNG in a 21-day Regimen.
Status: Enrolling
Updated:  12/31/1969
Agile Investigational Site
mi
from
Houston, TX
Study to Evaluate the Contraceptive Efficacy/Safety of a Low Dose EE/LNG Transdermal Contraceptive Delivery System
Open-label, Randomized, Parallel Group, Study of Efficacy and Safety of a Transdermal Contraceptive Delivery System (TCDS) in Comparison to a Low-dose Oral Contraceptive Containing 0.02 mg EE and 0.1 mg LNG in a 21-day Regimen.
Status: Enrolling
Updated: 12/31/1969
Agile Investigational Site
mi
from
Houston, TX
Click here to add this to my saved trials
Study to Evaluate the Contraceptive Efficacy/Safety of a Low Dose EE/LNG Transdermal Contraceptive Delivery System
Open-label, Randomized, Parallel Group, Study of Efficacy and Safety of a Transdermal Contraceptive Delivery System (TCDS) in Comparison to a Low-dose Oral Contraceptive Containing 0.02 mg EE and 0.1 mg LNG in a 21-day Regimen.
Status: Enrolling
Updated:  12/31/1969
Agile Investigational Site
mi
from
San Antonio, TX
Study to Evaluate the Contraceptive Efficacy/Safety of a Low Dose EE/LNG Transdermal Contraceptive Delivery System
Open-label, Randomized, Parallel Group, Study of Efficacy and Safety of a Transdermal Contraceptive Delivery System (TCDS) in Comparison to a Low-dose Oral Contraceptive Containing 0.02 mg EE and 0.1 mg LNG in a 21-day Regimen.
Status: Enrolling
Updated: 12/31/1969
Agile Investigational Site
mi
from
San Antonio, TX
Click here to add this to my saved trials
Study to Evaluate the Contraceptive Efficacy/Safety of a Low Dose EE/LNG Transdermal Contraceptive Delivery System
Open-label, Randomized, Parallel Group, Study of Efficacy and Safety of a Transdermal Contraceptive Delivery System (TCDS) in Comparison to a Low-dose Oral Contraceptive Containing 0.02 mg EE and 0.1 mg LNG in a 21-day Regimen.
Status: Enrolling
Updated:  12/31/1969
Agile Investigational Site
mi
from
Sugar Land, TX
Study to Evaluate the Contraceptive Efficacy/Safety of a Low Dose EE/LNG Transdermal Contraceptive Delivery System
Open-label, Randomized, Parallel Group, Study of Efficacy and Safety of a Transdermal Contraceptive Delivery System (TCDS) in Comparison to a Low-dose Oral Contraceptive Containing 0.02 mg EE and 0.1 mg LNG in a 21-day Regimen.
Status: Enrolling
Updated: 12/31/1969
Agile Investigational Site
mi
from
Sugar Land, TX
Click here to add this to my saved trials
Study to Evaluate the Contraceptive Efficacy/Safety of a Low Dose EE/LNG Transdermal Contraceptive Delivery System
Open-label, Randomized, Parallel Group, Study of Efficacy and Safety of a Transdermal Contraceptive Delivery System (TCDS) in Comparison to a Low-dose Oral Contraceptive Containing 0.02 mg EE and 0.1 mg LNG in a 21-day Regimen.
Status: Enrolling
Updated:  12/31/1969
Agile Investigational Site
mi
from
Webster, TX
Study to Evaluate the Contraceptive Efficacy/Safety of a Low Dose EE/LNG Transdermal Contraceptive Delivery System
Open-label, Randomized, Parallel Group, Study of Efficacy and Safety of a Transdermal Contraceptive Delivery System (TCDS) in Comparison to a Low-dose Oral Contraceptive Containing 0.02 mg EE and 0.1 mg LNG in a 21-day Regimen.
Status: Enrolling
Updated: 12/31/1969
Agile Investigational Site
mi
from
Webster, TX
Click here to add this to my saved trials
Study to Evaluate the Contraceptive Efficacy/Safety of a Low Dose EE/LNG Transdermal Contraceptive Delivery System
Open-label, Randomized, Parallel Group, Study of Efficacy and Safety of a Transdermal Contraceptive Delivery System (TCDS) in Comparison to a Low-dose Oral Contraceptive Containing 0.02 mg EE and 0.1 mg LNG in a 21-day Regimen.
Status: Enrolling
Updated:  12/31/1969
Agile Investigational Site
mi
from
Salt Lake City, UT
Study to Evaluate the Contraceptive Efficacy/Safety of a Low Dose EE/LNG Transdermal Contraceptive Delivery System
Open-label, Randomized, Parallel Group, Study of Efficacy and Safety of a Transdermal Contraceptive Delivery System (TCDS) in Comparison to a Low-dose Oral Contraceptive Containing 0.02 mg EE and 0.1 mg LNG in a 21-day Regimen.
Status: Enrolling
Updated: 12/31/1969
Agile Investigational Site
mi
from
Salt Lake City, UT
Click here to add this to my saved trials
Study to Evaluate the Contraceptive Efficacy/Safety of a Low Dose EE/LNG Transdermal Contraceptive Delivery System
Open-label, Randomized, Parallel Group, Study of Efficacy and Safety of a Transdermal Contraceptive Delivery System (TCDS) in Comparison to a Low-dose Oral Contraceptive Containing 0.02 mg EE and 0.1 mg LNG in a 21-day Regimen.
Status: Enrolling
Updated:  12/31/1969
Agile Investigational Site
mi
from
Newport News, VA
Study to Evaluate the Contraceptive Efficacy/Safety of a Low Dose EE/LNG Transdermal Contraceptive Delivery System
Open-label, Randomized, Parallel Group, Study of Efficacy and Safety of a Transdermal Contraceptive Delivery System (TCDS) in Comparison to a Low-dose Oral Contraceptive Containing 0.02 mg EE and 0.1 mg LNG in a 21-day Regimen.
Status: Enrolling
Updated: 12/31/1969
Agile Investigational Site
mi
from
Newport News, VA
Click here to add this to my saved trials
Study to Evaluate the Contraceptive Efficacy/Safety of a Low Dose EE/LNG Transdermal Contraceptive Delivery System
Open-label, Randomized, Parallel Group, Study of Efficacy and Safety of a Transdermal Contraceptive Delivery System (TCDS) in Comparison to a Low-dose Oral Contraceptive Containing 0.02 mg EE and 0.1 mg LNG in a 21-day Regimen.
Status: Enrolling
Updated:  12/31/1969
Agile Investigational Site
mi
from
Norfolk, VA
Study to Evaluate the Contraceptive Efficacy/Safety of a Low Dose EE/LNG Transdermal Contraceptive Delivery System
Open-label, Randomized, Parallel Group, Study of Efficacy and Safety of a Transdermal Contraceptive Delivery System (TCDS) in Comparison to a Low-dose Oral Contraceptive Containing 0.02 mg EE and 0.1 mg LNG in a 21-day Regimen.
Status: Enrolling
Updated: 12/31/1969
Agile Investigational Site
mi
from
Norfolk, VA
Click here to add this to my saved trials
Study to Evaluate the Contraceptive Efficacy/Safety of a Low Dose EE/LNG Transdermal Contraceptive Delivery System
Open-label, Randomized, Parallel Group, Study of Efficacy and Safety of a Transdermal Contraceptive Delivery System (TCDS) in Comparison to a Low-dose Oral Contraceptive Containing 0.02 mg EE and 0.1 mg LNG in a 21-day Regimen.
Status: Enrolling
Updated:  12/31/1969
Agile Investigational Site
mi
from
Richmond, VA
Study to Evaluate the Contraceptive Efficacy/Safety of a Low Dose EE/LNG Transdermal Contraceptive Delivery System
Open-label, Randomized, Parallel Group, Study of Efficacy and Safety of a Transdermal Contraceptive Delivery System (TCDS) in Comparison to a Low-dose Oral Contraceptive Containing 0.02 mg EE and 0.1 mg LNG in a 21-day Regimen.
Status: Enrolling
Updated: 12/31/1969
Agile Investigational Site
mi
from
Richmond, VA
Click here to add this to my saved trials
Study to Evaluate the Contraceptive Efficacy/Safety of a Low Dose EE/LNG Transdermal Contraceptive Delivery System
Open-label, Randomized, Parallel Group, Study of Efficacy and Safety of a Transdermal Contraceptive Delivery System (TCDS) in Comparison to a Low-dose Oral Contraceptive Containing 0.02 mg EE and 0.1 mg LNG in a 21-day Regimen.
Status: Enrolling
Updated:  12/31/1969
Agile Investigational Site
mi
from
Seattle, WA
Study to Evaluate the Contraceptive Efficacy/Safety of a Low Dose EE/LNG Transdermal Contraceptive Delivery System
Open-label, Randomized, Parallel Group, Study of Efficacy and Safety of a Transdermal Contraceptive Delivery System (TCDS) in Comparison to a Low-dose Oral Contraceptive Containing 0.02 mg EE and 0.1 mg LNG in a 21-day Regimen.
Status: Enrolling
Updated: 12/31/1969
Agile Investigational Site
mi
from
Seattle, WA
Click here to add this to my saved trials
Study to Evaluate the Contraceptive Efficacy/Safety of a Low Dose EE/LNG Transdermal Contraceptive Delivery System
Open-label, Randomized, Parallel Group, Study of Efficacy and Safety of a Transdermal Contraceptive Delivery System (TCDS) in Comparison to a Low-dose Oral Contraceptive Containing 0.02 mg EE and 0.1 mg LNG in a 21-day Regimen.
Status: Enrolling
Updated:  12/31/1969
Agile Investigational Site
mi
from
Tucson, AZ
Study to Evaluate the Contraceptive Efficacy/Safety of a Low Dose EE/LNG Transdermal Contraceptive Delivery System
Open-label, Randomized, Parallel Group, Study of Efficacy and Safety of a Transdermal Contraceptive Delivery System (TCDS) in Comparison to a Low-dose Oral Contraceptive Containing 0.02 mg EE and 0.1 mg LNG in a 21-day Regimen.
Status: Enrolling
Updated: 12/31/1969
Agile Investigational Site
mi
from
Tucson, AZ
Click here to add this to my saved trials
Study to Evaluate the Contraceptive Efficacy/Safety of a Low Dose EE/LNG Transdermal Contraceptive Delivery System
Open-label, Randomized, Parallel Group, Study of Efficacy and Safety of a Transdermal Contraceptive Delivery System (TCDS) in Comparison to a Low-dose Oral Contraceptive Containing 0.02 mg EE and 0.1 mg LNG in a 21-day Regimen.
Status: Enrolling
Updated:  12/31/1969
Agile Investigational Site
mi
from
Boynton Beach, FL
Study to Evaluate the Contraceptive Efficacy/Safety of a Low Dose EE/LNG Transdermal Contraceptive Delivery System
Open-label, Randomized, Parallel Group, Study of Efficacy and Safety of a Transdermal Contraceptive Delivery System (TCDS) in Comparison to a Low-dose Oral Contraceptive Containing 0.02 mg EE and 0.1 mg LNG in a 21-day Regimen.
Status: Enrolling
Updated: 12/31/1969
Agile Investigational Site
mi
from
Boynton Beach, FL
Click here to add this to my saved trials
Study to Evaluate the Contraceptive Efficacy/Safety of a Low Dose EE/LNG Transdermal Contraceptive Delivery System
Open-label, Randomized, Parallel Group, Study of Efficacy and Safety of a Transdermal Contraceptive Delivery System (TCDS) in Comparison to a Low-dose Oral Contraceptive Containing 0.02 mg EE and 0.1 mg LNG in a 21-day Regimen.
Status: Enrolling
Updated:  12/31/1969
Agile Investigational Site
mi
from
Saint Petersburg, FL
Study to Evaluate the Contraceptive Efficacy/Safety of a Low Dose EE/LNG Transdermal Contraceptive Delivery System
Open-label, Randomized, Parallel Group, Study of Efficacy and Safety of a Transdermal Contraceptive Delivery System (TCDS) in Comparison to a Low-dose Oral Contraceptive Containing 0.02 mg EE and 0.1 mg LNG in a 21-day Regimen.
Status: Enrolling
Updated: 12/31/1969
Agile Investigational Site
mi
from
Saint Petersburg, FL
Click here to add this to my saved trials
Safety and Expulsion of Delayed Versus Immediate Postpartum Intrauterine Device Placement
Safety and Expulsion of Delayed Versus Immediate Postpartum Intrauterine Device Placement: A Randomized, Controlled Trial
Status: Enrolling
Updated:  12/31/1969
University of Louisville
mi
from
Louisville, KY
Safety and Expulsion of Delayed Versus Immediate Postpartum Intrauterine Device Placement
Safety and Expulsion of Delayed Versus Immediate Postpartum Intrauterine Device Placement: A Randomized, Controlled Trial
Status: Enrolling
Updated: 12/31/1969
University of Louisville
mi
from
Louisville, KY
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E4 FREEDOM (Female Response Concerning Efficacy and Safety of Estetrol/Drospirenone as Oral Contraceptive in a Multicentric Study) - US/CA Study
A Multicenter, Open-label, Single-Arm Study to Evaluate the Contraceptive Efficacy and Safety of a Combined Oral Contraceptive Containing 15 mg Estetrol and 3 mg Drospirenone
Status: Enrolling
Updated:  12/31/1969
Thomas Jefferson University Obstetrics and Gynecology
mi
from
Philadelphia, PA
E4 FREEDOM (Female Response Concerning Efficacy and Safety of Estetrol/Drospirenone as Oral Contraceptive in a Multicentric Study) - US/CA Study
A Multicenter, Open-label, Single-Arm Study to Evaluate the Contraceptive Efficacy and Safety of a Combined Oral Contraceptive Containing 15 mg Estetrol and 3 mg Drospirenone
Status: Enrolling
Updated: 12/31/1969
Thomas Jefferson University Obstetrics and Gynecology
mi
from
Philadelphia, PA
Click here to add this to my saved trials
E4 FREEDOM (Female Response Concerning Efficacy and Safety of Estetrol/Drospirenone as Oral Contraceptive in a Multicentric Study) - US/CA Study
A Multicenter, Open-label, Single-Arm Study to Evaluate the Contraceptive Efficacy and Safety of a Combined Oral Contraceptive Containing 15 mg Estetrol and 3 mg Drospirenone
Status: Enrolling
Updated:  12/31/1969
Clinique de Santé des Femmes
mi
from
Quebec,
E4 FREEDOM (Female Response Concerning Efficacy and Safety of Estetrol/Drospirenone as Oral Contraceptive in a Multicentric Study) - US/CA Study
A Multicenter, Open-label, Single-Arm Study to Evaluate the Contraceptive Efficacy and Safety of a Combined Oral Contraceptive Containing 15 mg Estetrol and 3 mg Drospirenone
Status: Enrolling
Updated: 12/31/1969
Clinique de Santé des Femmes
mi
from
Quebec,
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Regulation of Cervical Mucus Secretion
Regulation of Cervical Mucus Secretion
Status: Enrolling
Updated:  12/31/1969
Oregon Health and Science University
mi
from
Portland, OR
Regulation of Cervical Mucus Secretion
Regulation of Cervical Mucus Secretion
Status: Enrolling
Updated: 12/31/1969
Oregon Health and Science University
mi
from
Portland, OR
Click here to add this to my saved trials
Perspectives on Prescribing Hormonal Contraception Among Rural New Mexicans
Perspectives on Prescribing Hormonal Contraception Among Rural New Mexicans
Status: Enrolling
Updated:  12/31/1969
Eve Espey
mi
from
Albuquerque, NM
Perspectives on Prescribing Hormonal Contraception Among Rural New Mexicans
Perspectives on Prescribing Hormonal Contraception Among Rural New Mexicans
Status: Enrolling
Updated: 12/31/1969
Eve Espey
mi
from
Albuquerque, NM
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A Comparison of Short Interval vs. Routine Postpartum Visit on Contraceptive Initiation
A Comparison of Short Interval vs. Routine Postpartum Visit on Contraceptive Initiation
Status: Enrolling
Updated:  12/31/1969
Washington University in St. Louis
mi
from
Saint Louis, MO
A Comparison of Short Interval vs. Routine Postpartum Visit on Contraceptive Initiation
A Comparison of Short Interval vs. Routine Postpartum Visit on Contraceptive Initiation
Status: Enrolling
Updated: 12/31/1969
Washington University in St. Louis
mi
from
Saint Louis, MO
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Nexplanon and Combined Oral Contraceptive (COC) Combined Use Study
Nexplanon Use in Women Primarily Choosing a Combined Hormonal Contraceptive: a Proof of Concept Trial
Status: Enrolling
Updated:  12/31/1969
University of California-Davis
mi
from
Sacramento, CA
Nexplanon and Combined Oral Contraceptive (COC) Combined Use Study
Nexplanon Use in Women Primarily Choosing a Combined Hormonal Contraceptive: a Proof of Concept Trial
Status: Enrolling
Updated: 12/31/1969
University of California-Davis
mi
from
Sacramento, CA
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Study of Self or Clinic Administration of DepoProvera
Randomized Clinical Trial of Self Versus Clinical Administration of Depot Medroxyprogesterone Acetate
Status: Enrolling
Updated:  12/31/1969
Columbia University, New York - Presbyterian Hospital
mi
from
New York, NY
Study of Self or Clinic Administration of DepoProvera
Randomized Clinical Trial of Self Versus Clinical Administration of Depot Medroxyprogesterone Acetate
Status: Enrolling
Updated: 12/31/1969
Columbia University, New York - Presbyterian Hospital
mi
from
New York, NY
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KYleena Satisfaction Study / Observational Study on User Satisfaction With the Levonorgestrel Intrauterine Delivery System Kyleena (LNG-IUS 12) in New Contraceptive Users and After Switching From Another Contraceptive Method
KYleena Satisfaction Study / Observational Study on User Satisfaction With the Levonorgestrel Intrauterine Delivery System Kyleena (LNG-IUS 12) in New Contraceptive Users and After Switching From Another Contraceptive Method
Status: Enrolling
Updated:  12/31/1969
Jennifer Grube, MD, FACOG
mi
from
Lakewood, CO
KYleena Satisfaction Study / Observational Study on User Satisfaction With the Levonorgestrel Intrauterine Delivery System Kyleena (LNG-IUS 12) in New Contraceptive Users and After Switching From Another Contraceptive Method
KYleena Satisfaction Study / Observational Study on User Satisfaction With the Levonorgestrel Intrauterine Delivery System Kyleena (LNG-IUS 12) in New Contraceptive Users and After Switching From Another Contraceptive Method
Status: Enrolling
Updated: 12/31/1969
Jennifer Grube, MD, FACOG
mi
from
Lakewood, CO
Click here to add this to my saved trials
KYleena Satisfaction Study / Observational Study on User Satisfaction With the Levonorgestrel Intrauterine Delivery System Kyleena (LNG-IUS 12) in New Contraceptive Users and After Switching From Another Contraceptive Method
KYleena Satisfaction Study / Observational Study on User Satisfaction With the Levonorgestrel Intrauterine Delivery System Kyleena (LNG-IUS 12) in New Contraceptive Users and After Switching From Another Contraceptive Method
Status: Enrolling
Updated:  12/31/1969
Physician Care Clinical Research, LLC
mi
from
Sarasota, FL
KYleena Satisfaction Study / Observational Study on User Satisfaction With the Levonorgestrel Intrauterine Delivery System Kyleena (LNG-IUS 12) in New Contraceptive Users and After Switching From Another Contraceptive Method
KYleena Satisfaction Study / Observational Study on User Satisfaction With the Levonorgestrel Intrauterine Delivery System Kyleena (LNG-IUS 12) in New Contraceptive Users and After Switching From Another Contraceptive Method
Status: Enrolling
Updated: 12/31/1969
Physician Care Clinical Research, LLC
mi
from
Sarasota, FL
Click here to add this to my saved trials
KYleena Satisfaction Study / Observational Study on User Satisfaction With the Levonorgestrel Intrauterine Delivery System Kyleena (LNG-IUS 12) in New Contraceptive Users and After Switching From Another Contraceptive Method
KYleena Satisfaction Study / Observational Study on User Satisfaction With the Levonorgestrel Intrauterine Delivery System Kyleena (LNG-IUS 12) in New Contraceptive Users and After Switching From Another Contraceptive Method
Status: Enrolling
Updated:  12/31/1969
Visions Clinical Research
mi
from
Wellington, FL
KYleena Satisfaction Study / Observational Study on User Satisfaction With the Levonorgestrel Intrauterine Delivery System Kyleena (LNG-IUS 12) in New Contraceptive Users and After Switching From Another Contraceptive Method
KYleena Satisfaction Study / Observational Study on User Satisfaction With the Levonorgestrel Intrauterine Delivery System Kyleena (LNG-IUS 12) in New Contraceptive Users and After Switching From Another Contraceptive Method
Status: Enrolling
Updated: 12/31/1969
Visions Clinical Research
mi
from
Wellington, FL
Click here to add this to my saved trials
KYleena Satisfaction Study / Observational Study on User Satisfaction With the Levonorgestrel Intrauterine Delivery System Kyleena (LNG-IUS 12) in New Contraceptive Users and After Switching From Another Contraceptive Method
KYleena Satisfaction Study / Observational Study on User Satisfaction With the Levonorgestrel Intrauterine Delivery System Kyleena (LNG-IUS 12) in New Contraceptive Users and After Switching From Another Contraceptive Method
Status: Enrolling
Updated:  12/31/1969
New England Center for Clinical Research Primacare Research, LLC
mi
from
Fall River, MA
KYleena Satisfaction Study / Observational Study on User Satisfaction With the Levonorgestrel Intrauterine Delivery System Kyleena (LNG-IUS 12) in New Contraceptive Users and After Switching From Another Contraceptive Method
KYleena Satisfaction Study / Observational Study on User Satisfaction With the Levonorgestrel Intrauterine Delivery System Kyleena (LNG-IUS 12) in New Contraceptive Users and After Switching From Another Contraceptive Method
Status: Enrolling
Updated: 12/31/1969
New England Center for Clinical Research Primacare Research, LLC
mi
from
Fall River, MA
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KYleena Satisfaction Study / Observational Study on User Satisfaction With the Levonorgestrel Intrauterine Delivery System Kyleena (LNG-IUS 12) in New Contraceptive Users and After Switching From Another Contraceptive Method
KYleena Satisfaction Study / Observational Study on User Satisfaction With the Levonorgestrel Intrauterine Delivery System Kyleena (LNG-IUS 12) in New Contraceptive Users and After Switching From Another Contraceptive Method
Status: Enrolling
Updated:  12/31/1969
Saginaw Valley Medical Research Group, LLC
mi
from
Saginaw, MI
KYleena Satisfaction Study / Observational Study on User Satisfaction With the Levonorgestrel Intrauterine Delivery System Kyleena (LNG-IUS 12) in New Contraceptive Users and After Switching From Another Contraceptive Method
KYleena Satisfaction Study / Observational Study on User Satisfaction With the Levonorgestrel Intrauterine Delivery System Kyleena (LNG-IUS 12) in New Contraceptive Users and After Switching From Another Contraceptive Method
Status: Enrolling
Updated: 12/31/1969
Saginaw Valley Medical Research Group, LLC
mi
from
Saginaw, MI
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KYleena Satisfaction Study / Observational Study on User Satisfaction With the Levonorgestrel Intrauterine Delivery System Kyleena (LNG-IUS 12) in New Contraceptive Users and After Switching From Another Contraceptive Method
KYleena Satisfaction Study / Observational Study on User Satisfaction With the Levonorgestrel Intrauterine Delivery System Kyleena (LNG-IUS 12) in New Contraceptive Users and After Switching From Another Contraceptive Method
Status: Enrolling
Updated:  12/31/1969
Lawrence OB-GYN Clinical Research, LLC
mi
from
Lawrenceville, NJ
KYleena Satisfaction Study / Observational Study on User Satisfaction With the Levonorgestrel Intrauterine Delivery System Kyleena (LNG-IUS 12) in New Contraceptive Users and After Switching From Another Contraceptive Method
KYleena Satisfaction Study / Observational Study on User Satisfaction With the Levonorgestrel Intrauterine Delivery System Kyleena (LNG-IUS 12) in New Contraceptive Users and After Switching From Another Contraceptive Method
Status: Enrolling
Updated: 12/31/1969
Lawrence OB-GYN Clinical Research, LLC
mi
from
Lawrenceville, NJ
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KYleena Satisfaction Study / Observational Study on User Satisfaction With the Levonorgestrel Intrauterine Delivery System Kyleena (LNG-IUS 12) in New Contraceptive Users and After Switching From Another Contraceptive Method
KYleena Satisfaction Study / Observational Study on User Satisfaction With the Levonorgestrel Intrauterine Delivery System Kyleena (LNG-IUS 12) in New Contraceptive Users and After Switching From Another Contraceptive Method
Status: Enrolling
Updated:  12/31/1969
ProHEALTH Care Associates
mi
from
Port Jefferson, NY
KYleena Satisfaction Study / Observational Study on User Satisfaction With the Levonorgestrel Intrauterine Delivery System Kyleena (LNG-IUS 12) in New Contraceptive Users and After Switching From Another Contraceptive Method
KYleena Satisfaction Study / Observational Study on User Satisfaction With the Levonorgestrel Intrauterine Delivery System Kyleena (LNG-IUS 12) in New Contraceptive Users and After Switching From Another Contraceptive Method
Status: Enrolling
Updated: 12/31/1969
ProHEALTH Care Associates
mi
from
Port Jefferson, NY
Click here to add this to my saved trials
KYleena Satisfaction Study / Observational Study on User Satisfaction With the Levonorgestrel Intrauterine Delivery System Kyleena (LNG-IUS 12) in New Contraceptive Users and After Switching From Another Contraceptive Method
KYleena Satisfaction Study / Observational Study on User Satisfaction With the Levonorgestrel Intrauterine Delivery System Kyleena (LNG-IUS 12) in New Contraceptive Users and After Switching From Another Contraceptive Method
Status: Enrolling
Updated:  12/31/1969
Eastern Carolina Women's Center
mi
from
New Bern, NC
KYleena Satisfaction Study / Observational Study on User Satisfaction With the Levonorgestrel Intrauterine Delivery System Kyleena (LNG-IUS 12) in New Contraceptive Users and After Switching From Another Contraceptive Method
KYleena Satisfaction Study / Observational Study on User Satisfaction With the Levonorgestrel Intrauterine Delivery System Kyleena (LNG-IUS 12) in New Contraceptive Users and After Switching From Another Contraceptive Method
Status: Enrolling
Updated: 12/31/1969
Eastern Carolina Women's Center
mi
from
New Bern, NC
Click here to add this to my saved trials
KYleena Satisfaction Study / Observational Study on User Satisfaction With the Levonorgestrel Intrauterine Delivery System Kyleena (LNG-IUS 12) in New Contraceptive Users and After Switching From Another Contraceptive Method
KYleena Satisfaction Study / Observational Study on User Satisfaction With the Levonorgestrel Intrauterine Delivery System Kyleena (LNG-IUS 12) in New Contraceptive Users and After Switching From Another Contraceptive Method
Status: Enrolling
Updated:  12/31/1969
Radiant Research, Inc.
mi
from
Akron, OH
KYleena Satisfaction Study / Observational Study on User Satisfaction With the Levonorgestrel Intrauterine Delivery System Kyleena (LNG-IUS 12) in New Contraceptive Users and After Switching From Another Contraceptive Method
KYleena Satisfaction Study / Observational Study on User Satisfaction With the Levonorgestrel Intrauterine Delivery System Kyleena (LNG-IUS 12) in New Contraceptive Users and After Switching From Another Contraceptive Method
Status: Enrolling
Updated: 12/31/1969
Radiant Research, Inc.
mi
from
Akron, OH
Click here to add this to my saved trials
KYleena Satisfaction Study / Observational Study on User Satisfaction With the Levonorgestrel Intrauterine Delivery System Kyleena (LNG-IUS 12) in New Contraceptive Users and After Switching From Another Contraceptive Method
KYleena Satisfaction Study / Observational Study on User Satisfaction With the Levonorgestrel Intrauterine Delivery System Kyleena (LNG-IUS 12) in New Contraceptive Users and After Switching From Another Contraceptive Method
Status: Enrolling
Updated:  12/31/1969
TMC Life Research, Inc
mi
from
Houston, TX
KYleena Satisfaction Study / Observational Study on User Satisfaction With the Levonorgestrel Intrauterine Delivery System Kyleena (LNG-IUS 12) in New Contraceptive Users and After Switching From Another Contraceptive Method
KYleena Satisfaction Study / Observational Study on User Satisfaction With the Levonorgestrel Intrauterine Delivery System Kyleena (LNG-IUS 12) in New Contraceptive Users and After Switching From Another Contraceptive Method
Status: Enrolling
Updated: 12/31/1969
TMC Life Research, Inc
mi
from
Houston, TX
Click here to add this to my saved trials
KYleena Satisfaction Study / Observational Study on User Satisfaction With the Levonorgestrel Intrauterine Delivery System Kyleena (LNG-IUS 12) in New Contraceptive Users and After Switching From Another Contraceptive Method
KYleena Satisfaction Study / Observational Study on User Satisfaction With the Levonorgestrel Intrauterine Delivery System Kyleena (LNG-IUS 12) in New Contraceptive Users and After Switching From Another Contraceptive Method
Status: Enrolling
Updated:  12/31/1969
Physician's Research
mi
from
Draper, UT
KYleena Satisfaction Study / Observational Study on User Satisfaction With the Levonorgestrel Intrauterine Delivery System Kyleena (LNG-IUS 12) in New Contraceptive Users and After Switching From Another Contraceptive Method
KYleena Satisfaction Study / Observational Study on User Satisfaction With the Levonorgestrel Intrauterine Delivery System Kyleena (LNG-IUS 12) in New Contraceptive Users and After Switching From Another Contraceptive Method
Status: Enrolling
Updated: 12/31/1969
Physician's Research
mi
from
Draper, UT
Click here to add this to my saved trials
KYleena Satisfaction Study / Observational Study on User Satisfaction With the Levonorgestrel Intrauterine Delivery System Kyleena (LNG-IUS 12) in New Contraceptive Users and After Switching From Another Contraceptive Method
KYleena Satisfaction Study / Observational Study on User Satisfaction With the Levonorgestrel Intrauterine Delivery System Kyleena (LNG-IUS 12) in New Contraceptive Users and After Switching From Another Contraceptive Method
Status: Enrolling
Updated:  12/31/1969
Physician's Research Options LLC - Revere Women's Health OB/GYN Clinic
mi
from
Pleasant Grove, UT
KYleena Satisfaction Study / Observational Study on User Satisfaction With the Levonorgestrel Intrauterine Delivery System Kyleena (LNG-IUS 12) in New Contraceptive Users and After Switching From Another Contraceptive Method
KYleena Satisfaction Study / Observational Study on User Satisfaction With the Levonorgestrel Intrauterine Delivery System Kyleena (LNG-IUS 12) in New Contraceptive Users and After Switching From Another Contraceptive Method
Status: Enrolling
Updated: 12/31/1969
Physician's Research Options LLC - Revere Women's Health OB/GYN Clinic
mi
from
Pleasant Grove, UT
Click here to add this to my saved trials
KYleena Satisfaction Study / Observational Study on User Satisfaction With the Levonorgestrel Intrauterine Delivery System Kyleena (LNG-IUS 12) in New Contraceptive Users and After Switching From Another Contraceptive Method
KYleena Satisfaction Study / Observational Study on User Satisfaction With the Levonorgestrel Intrauterine Delivery System Kyleena (LNG-IUS 12) in New Contraceptive Users and After Switching From Another Contraceptive Method
Status: Enrolling
Updated:  12/31/1969
Many locations
mi
from
Multiple Locations,
KYleena Satisfaction Study / Observational Study on User Satisfaction With the Levonorgestrel Intrauterine Delivery System Kyleena (LNG-IUS 12) in New Contraceptive Users and After Switching From Another Contraceptive Method
KYleena Satisfaction Study / Observational Study on User Satisfaction With the Levonorgestrel Intrauterine Delivery System Kyleena (LNG-IUS 12) in New Contraceptive Users and After Switching From Another Contraceptive Method
Status: Enrolling
Updated: 12/31/1969
Many locations
mi
from
Multiple Locations,
Click here to add this to my saved trials
Family Planning Ahead
Family Planning Ahead
Status: Enrolling
Updated:  12/31/1969
Internet (Dartmouth College)
mi
from
Lebanon, NH
Family Planning Ahead
Family Planning Ahead
Status: Enrolling
Updated: 12/31/1969
Internet (Dartmouth College)
mi
from
Lebanon, NH
Click here to add this to my saved trials
A Study of Oral Contraception Under Simulated OTC Conditions
A Multi-Center Oral Contraceptive Pill Use Trial Conducted In an OTC Naturalistic Environment (OPTION)
Status: Enrolling
Updated:  12/31/1969
HRA Pharma Investigational site
mi
from
Birmingham, AL
A Study of Oral Contraception Under Simulated OTC Conditions
A Multi-Center Oral Contraceptive Pill Use Trial Conducted In an OTC Naturalistic Environment (OPTION)
Status: Enrolling
Updated: 12/31/1969
HRA Pharma Investigational site
mi
from
Birmingham, AL
Click here to add this to my saved trials
A Study of Oral Contraception Under Simulated OTC Conditions
A Multi-Center Oral Contraceptive Pill Use Trial Conducted In an OTC Naturalistic Environment (OPTION)
Status: Enrolling
Updated:  12/31/1969
HRA Pharma Investigational site
mi
from
Homewood, AL
A Study of Oral Contraception Under Simulated OTC Conditions
A Multi-Center Oral Contraceptive Pill Use Trial Conducted In an OTC Naturalistic Environment (OPTION)
Status: Enrolling
Updated: 12/31/1969
HRA Pharma Investigational site
mi
from
Homewood, AL
Click here to add this to my saved trials
A Study of Oral Contraception Under Simulated OTC Conditions
A Multi-Center Oral Contraceptive Pill Use Trial Conducted In an OTC Naturalistic Environment (OPTION)
Status: Enrolling
Updated:  12/31/1969
HRA Pharma Investigational site
mi
from
McCalla, AL
A Study of Oral Contraception Under Simulated OTC Conditions
A Multi-Center Oral Contraceptive Pill Use Trial Conducted In an OTC Naturalistic Environment (OPTION)
Status: Enrolling
Updated: 12/31/1969
HRA Pharma Investigational site
mi
from
McCalla, AL
Click here to add this to my saved trials
A Study of Oral Contraception Under Simulated OTC Conditions
A Multi-Center Oral Contraceptive Pill Use Trial Conducted In an OTC Naturalistic Environment (OPTION)
Status: Enrolling
Updated:  12/31/1969
HRA Pharma Investigational site
mi
from
Tucson, AZ
A Study of Oral Contraception Under Simulated OTC Conditions
A Multi-Center Oral Contraceptive Pill Use Trial Conducted In an OTC Naturalistic Environment (OPTION)
Status: Enrolling
Updated: 12/31/1969
HRA Pharma Investigational site
mi
from
Tucson, AZ
Click here to add this to my saved trials
A Study of Oral Contraception Under Simulated OTC Conditions
A Multi-Center Oral Contraceptive Pill Use Trial Conducted In an OTC Naturalistic Environment (OPTION)
Status: Enrolling
Updated:  12/31/1969
HRA Pharma Investigational site
mi
from
Downey, CA
A Study of Oral Contraception Under Simulated OTC Conditions
A Multi-Center Oral Contraceptive Pill Use Trial Conducted In an OTC Naturalistic Environment (OPTION)
Status: Enrolling
Updated: 12/31/1969
HRA Pharma Investigational site
mi
from
Downey, CA
Click here to add this to my saved trials
A Study of Oral Contraception Under Simulated OTC Conditions
A Multi-Center Oral Contraceptive Pill Use Trial Conducted In an OTC Naturalistic Environment (OPTION)
Status: Enrolling
Updated:  12/31/1969
HRA Pharma Investigational site
mi
from
La Habra, CA
A Study of Oral Contraception Under Simulated OTC Conditions
A Multi-Center Oral Contraceptive Pill Use Trial Conducted In an OTC Naturalistic Environment (OPTION)
Status: Enrolling
Updated: 12/31/1969
HRA Pharma Investigational site
mi
from
La Habra, CA
Click here to add this to my saved trials
A Study of Oral Contraception Under Simulated OTC Conditions
A Multi-Center Oral Contraceptive Pill Use Trial Conducted In an OTC Naturalistic Environment (OPTION)
Status: Enrolling
Updated:  12/31/1969
HRA Pharma Investigational site
mi
from
Long Beach, CA
A Study of Oral Contraception Under Simulated OTC Conditions
A Multi-Center Oral Contraceptive Pill Use Trial Conducted In an OTC Naturalistic Environment (OPTION)
Status: Enrolling
Updated: 12/31/1969
HRA Pharma Investigational site
mi
from
Long Beach, CA
Click here to add this to my saved trials
A Study of Oral Contraception Under Simulated OTC Conditions
A Multi-Center Oral Contraceptive Pill Use Trial Conducted In an OTC Naturalistic Environment (OPTION)
Status: Enrolling
Updated:  12/31/1969
HRA Pharma Investigational site
mi
from
Los Angeles, CA
A Study of Oral Contraception Under Simulated OTC Conditions
A Multi-Center Oral Contraceptive Pill Use Trial Conducted In an OTC Naturalistic Environment (OPTION)
Status: Enrolling
Updated: 12/31/1969
HRA Pharma Investigational site
mi
from
Los Angeles, CA
Click here to add this to my saved trials
A Study of Oral Contraception Under Simulated OTC Conditions
A Multi-Center Oral Contraceptive Pill Use Trial Conducted In an OTC Naturalistic Environment (OPTION)
Status: Enrolling
Updated:  12/31/1969
HRA Pharma Investigational site
mi
from
Bridgeport, CT
A Study of Oral Contraception Under Simulated OTC Conditions
A Multi-Center Oral Contraceptive Pill Use Trial Conducted In an OTC Naturalistic Environment (OPTION)
Status: Enrolling
Updated: 12/31/1969
HRA Pharma Investigational site
mi
from
Bridgeport, CT
Click here to add this to my saved trials