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.

Zip code

Condition


Search Radius:25 Miles
  • 5
  • 10
  • 15
  • 20
  • 25
  • 30
  • 40
  • 50
  • 100
  • 500
  • All

We've found
821
archived clinical trials in
Contraception

Essure (Model ESS310) Placement Rate Study
A Multi-Center, United States Clinical Study to Evaluate Placement Success of the ESS310 Essure® System
Status: Enrolling
Updated:  12/14/2015
Clinical Research Facility
mi
from
Newburgh, IN
Essure (Model ESS310) Placement Rate Study
A Multi-Center, United States Clinical Study to Evaluate Placement Success of the ESS310 Essure® System
Status: Enrolling
Updated: 12/14/2015
Clinical Research Facility
mi
from
Newburgh, IN
Click here to add this to my saved trials
Essure (Model ESS310) Placement Rate Study
A Multi-Center, United States Clinical Study to Evaluate Placement Success of the ESS310 Essure® System
Status: Enrolling
Updated:  12/14/2015
Clinical Research Facility
mi
from
Grand Blanc, MI
Essure (Model ESS310) Placement Rate Study
A Multi-Center, United States Clinical Study to Evaluate Placement Success of the ESS310 Essure® System
Status: Enrolling
Updated: 12/14/2015
Clinical Research Facility
mi
from
Grand Blanc, MI
Click here to add this to my saved trials
Essure (Model ESS310) Placement Rate Study
A Multi-Center, United States Clinical Study to Evaluate Placement Success of the ESS310 Essure® System
Status: Enrolling
Updated:  12/14/2015
Clinical Research Facility
mi
from
Saginaw, MI
Essure (Model ESS310) Placement Rate Study
A Multi-Center, United States Clinical Study to Evaluate Placement Success of the ESS310 Essure® System
Status: Enrolling
Updated: 12/14/2015
Clinical Research Facility
mi
from
Saginaw, MI
Click here to add this to my saved trials
Essure (Model ESS310) Placement Rate Study
A Multi-Center, United States Clinical Study to Evaluate Placement Success of the ESS310 Essure® System
Status: Enrolling
Updated:  12/14/2015
Clinical Research Facility
mi
from
Southfield, MI
Essure (Model ESS310) Placement Rate Study
A Multi-Center, United States Clinical Study to Evaluate Placement Success of the ESS310 Essure® System
Status: Enrolling
Updated: 12/14/2015
Clinical Research Facility
mi
from
Southfield, MI
Click here to add this to my saved trials
Essure (Model ESS310) Placement Rate Study
A Multi-Center, United States Clinical Study to Evaluate Placement Success of the ESS310 Essure® System
Status: Enrolling
Updated:  12/14/2015
Clinical Research Facility
mi
from
Rochester, MN
Essure (Model ESS310) Placement Rate Study
A Multi-Center, United States Clinical Study to Evaluate Placement Success of the ESS310 Essure® System
Status: Enrolling
Updated: 12/14/2015
Clinical Research Facility
mi
from
Rochester, MN
Click here to add this to my saved trials
Essure (Model ESS310) Placement Rate Study
A Multi-Center, United States Clinical Study to Evaluate Placement Success of the ESS310 Essure® System
Status: Enrolling
Updated:  12/14/2015
Clinical Research Facility
mi
from
Winston-Salem, NC
Essure (Model ESS310) Placement Rate Study
A Multi-Center, United States Clinical Study to Evaluate Placement Success of the ESS310 Essure® System
Status: Enrolling
Updated: 12/14/2015
Clinical Research Facility
mi
from
Winston-Salem, NC
Click here to add this to my saved trials
Essure (Model ESS310) Placement Rate Study
A Multi-Center, United States Clinical Study to Evaluate Placement Success of the ESS310 Essure® System
Status: Enrolling
Updated:  12/14/2015
Clinical Research Facility
mi
from
Dayton, OH
Essure (Model ESS310) Placement Rate Study
A Multi-Center, United States Clinical Study to Evaluate Placement Success of the ESS310 Essure® System
Status: Enrolling
Updated: 12/14/2015
Clinical Research Facility
mi
from
Dayton, OH
Click here to add this to my saved trials
Essure (Model ESS310) Placement Rate Study
A Multi-Center, United States Clinical Study to Evaluate Placement Success of the ESS310 Essure® System
Status: Enrolling
Updated:  12/14/2015
Clinical Research Facility
mi
from
Nashville, TN
Essure (Model ESS310) Placement Rate Study
A Multi-Center, United States Clinical Study to Evaluate Placement Success of the ESS310 Essure® System
Status: Enrolling
Updated: 12/14/2015
Clinical Research Facility
mi
from
Nashville, TN
Click here to add this to my saved trials
Essure (Model ESS310) Placement Rate Study
A Multi-Center, United States Clinical Study to Evaluate Placement Success of the ESS310 Essure® System
Status: Enrolling
Updated:  12/14/2015
Clinical Research Facility
mi
from
Nashville, TN
Essure (Model ESS310) Placement Rate Study
A Multi-Center, United States Clinical Study to Evaluate Placement Success of the ESS310 Essure® System
Status: Enrolling
Updated: 12/14/2015
Clinical Research Facility
mi
from
Nashville, TN
Click here to add this to my saved trials
Essure (Model ESS310) Placement Rate Study
A Multi-Center, United States Clinical Study to Evaluate Placement Success of the ESS310 Essure® System
Status: Enrolling
Updated:  12/14/2015
Clinical Research Facility
mi
from
Fort Worth, TX
Essure (Model ESS310) Placement Rate Study
A Multi-Center, United States Clinical Study to Evaluate Placement Success of the ESS310 Essure® System
Status: Enrolling
Updated: 12/14/2015
Clinical Research Facility
mi
from
Fort Worth, TX
Click here to add this to my saved trials
Essure (Model ESS310) Placement Rate Study
A Multi-Center, United States Clinical Study to Evaluate Placement Success of the ESS310 Essure® System
Status: Enrolling
Updated:  12/14/2015
Clinical Research Facility
mi
from
Houston, TX
Essure (Model ESS310) Placement Rate Study
A Multi-Center, United States Clinical Study to Evaluate Placement Success of the ESS310 Essure® System
Status: Enrolling
Updated: 12/14/2015
Clinical Research Facility
mi
from
Houston, TX
Click here to add this to my saved trials
Women With Epilepsy: a Pilot Study of PK and PD Anti-epileptic Drug Effects in Levonorgestrel Intrauterine System Users
Women With Epilepsy: a Pilot Study of Pharmacokinetic and Pharmacodynamic Anti-epileptic Drug Effects in Levonorgestrel Intrauterine System Users
Status: Enrolling
Updated:  12/14/2015
Columbia University
mi
from
New York, NY
Women With Epilepsy: a Pilot Study of PK and PD Anti-epileptic Drug Effects in Levonorgestrel Intrauterine System Users
Women With Epilepsy: a Pilot Study of Pharmacokinetic and Pharmacodynamic Anti-epileptic Drug Effects in Levonorgestrel Intrauterine System Users
Status: Enrolling
Updated: 12/14/2015
Columbia University
mi
from
New York, NY
Click here to add this to my saved trials
Nitrous Oxide for Pain Management of Intrauterine Device (IUD) Insertion
Nitrous Oxide for Pain Management of Intrauterine Device Insertion
Status: Enrolling
Updated:  1/4/2016
Center for Reproductive Health
mi
from
Albuquerque, NM
Nitrous Oxide for Pain Management of Intrauterine Device (IUD) Insertion
Nitrous Oxide for Pain Management of Intrauterine Device Insertion
Status: Enrolling
Updated: 1/4/2016
Center for Reproductive Health
mi
from
Albuquerque, NM
Click here to add this to my saved trials
Phase I One-month Safety, PK, PD, and Acceptability Study of IVR Releasing TFV and LNG or TFV Alone
Phase I One-Month Safety, Pharmacokinetic, Pharmacodynamic, and Acceptability Study of Intravaginal Rings Releasing Tenofovir and Levonorgestrel or Tenofovir Alone
Status: Enrolling
Updated:  1/8/2016
Eastern Virginia Medical School
mi
from
Norfolk, VA
Phase I One-month Safety, PK, PD, and Acceptability Study of IVR Releasing TFV and LNG or TFV Alone
Phase I One-Month Safety, Pharmacokinetic, Pharmacodynamic, and Acceptability Study of Intravaginal Rings Releasing Tenofovir and Levonorgestrel or Tenofovir Alone
Status: Enrolling
Updated: 1/8/2016
Eastern Virginia Medical School
mi
from
Norfolk, VA
Click here to add this to my saved trials
Phase I One-month Safety, PK, PD, and Acceptability Study of IVR Releasing TFV and LNG or TFV Alone
Phase I One-Month Safety, Pharmacokinetic, Pharmacodynamic, and Acceptability Study of Intravaginal Rings Releasing Tenofovir and Levonorgestrel or Tenofovir Alone
Status: Enrolling
Updated:  1/8/2016
Profamilia
mi
from
Santo Domingo,
Phase I One-month Safety, PK, PD, and Acceptability Study of IVR Releasing TFV and LNG or TFV Alone
Phase I One-Month Safety, Pharmacokinetic, Pharmacodynamic, and Acceptability Study of Intravaginal Rings Releasing Tenofovir and Levonorgestrel or Tenofovir Alone
Status: Enrolling
Updated: 1/8/2016
Profamilia
mi
from
Santo Domingo,
Click here to add this to my saved trials
Postcoital Testing Study of the SILCS Diaphragm Used With 3% N-9 Gel, ContraGel, or No Gel
A Phase I Postcoital Testing Study of the SILCS Diaphragm Used With 3% Nonoxynol-9 Gel, ContraGel, or No Gel
Status: Enrolling
Updated:  1/8/2016
Clinical Research Center at Eastern Virginia Medical School
mi
from
Norfolk, VA
Postcoital Testing Study of the SILCS Diaphragm Used With 3% N-9 Gel, ContraGel, or No Gel
A Phase I Postcoital Testing Study of the SILCS Diaphragm Used With 3% Nonoxynol-9 Gel, ContraGel, or No Gel
Status: Enrolling
Updated: 1/8/2016
Clinical Research Center at Eastern Virginia Medical School
mi
from
Norfolk, VA
Click here to add this to my saved trials
Postcoital Testing Study of the SILCS Diaphragm Used With 3% N-9 Gel, ContraGel, or No Gel
A Phase I Postcoital Testing Study of the SILCS Diaphragm Used With 3% Nonoxynol-9 Gel, ContraGel, or No Gel
Status: Enrolling
Updated:  1/8/2016
Profamilia
mi
from
Santo Domingo,
Postcoital Testing Study of the SILCS Diaphragm Used With 3% N-9 Gel, ContraGel, or No Gel
A Phase I Postcoital Testing Study of the SILCS Diaphragm Used With 3% Nonoxynol-9 Gel, ContraGel, or No Gel
Status: Enrolling
Updated: 1/8/2016
Profamilia
mi
from
Santo Domingo,
Click here to add this to my saved trials
Changes in Vaginal, Cervical and Uterine Microflora With Levonorgestrel Intrauterine Device Placement
Vaginal Microflora and Inflammatory Markers Before and After Levonorgestrel Device Insertion
Status: Enrolling
Updated:  1/11/2016
University Of Utah Hospital
mi
from
Salt Lake City, UT
Changes in Vaginal, Cervical and Uterine Microflora With Levonorgestrel Intrauterine Device Placement
Vaginal Microflora and Inflammatory Markers Before and After Levonorgestrel Device Insertion
Status: Enrolling
Updated: 1/11/2016
University Of Utah Hospital
mi
from
Salt Lake City, UT
Click here to add this to my saved trials
Postplacental or Delayed Insertion of the Levonorgestrel-releasing Intrauterine Device (IUD) After Vaginal Delivery
Randomized Trial of Postplacental or Delayed Insertion of the Levonorgestrel-releasing Intrauterine Device After Vaginal Delivery
Status: Enrolling
Updated:  1/22/2016
Magee-Womens Hospital, University of Pittsburgh
mi
from
Pittsburgh, PA
Postplacental or Delayed Insertion of the Levonorgestrel-releasing Intrauterine Device (IUD) After Vaginal Delivery
Randomized Trial of Postplacental or Delayed Insertion of the Levonorgestrel-releasing Intrauterine Device After Vaginal Delivery
Status: Enrolling
Updated: 1/22/2016
Magee-Womens Hospital, University of Pittsburgh
mi
from
Pittsburgh, PA
Click here to add this to my saved trials
A Multi-center, Open-label, Randomized, Parallel Group Study to Evaluate Pharmacokinetic Profile, Effects on the Mechanisms of Contraceptive Efficacy and Safety of Two Progestin-only Patches Containing Different Doses of Levonorgestrel (LNG)
CCN009: A Multi-center, Open-label, Randomized, Parallel Group Study to Evaluate the Effects on the Mechanisms of Contraceptive Efficacy and, Secondarily, to Assess the Pharmacokinetic Profile and Safety of Two Progestin-only Patches Containing Different Doses of Levonorgestrel (LNG)
Status: Enrolling
Updated:  2/19/2016
University of Colorado - Adv. Repro. Med.
mi
from
Aurora, CO
A Multi-center, Open-label, Randomized, Parallel Group Study to Evaluate Pharmacokinetic Profile, Effects on the Mechanisms of Contraceptive Efficacy and Safety of Two Progestin-only Patches Containing Different Doses of Levonorgestrel (LNG)
CCN009: A Multi-center, Open-label, Randomized, Parallel Group Study to Evaluate the Effects on the Mechanisms of Contraceptive Efficacy and, Secondarily, to Assess the Pharmacokinetic Profile and Safety of Two Progestin-only Patches Containing Different Doses of Levonorgestrel (LNG)
Status: Enrolling
Updated: 2/19/2016
University of Colorado - Adv. Repro. Med.
mi
from
Aurora, CO
Click here to add this to my saved trials
A Multi-center, Open-label, Randomized, Parallel Group Study to Evaluate Pharmacokinetic Profile, Effects on the Mechanisms of Contraceptive Efficacy and Safety of Two Progestin-only Patches Containing Different Doses of Levonorgestrel (LNG)
CCN009: A Multi-center, Open-label, Randomized, Parallel Group Study to Evaluate the Effects on the Mechanisms of Contraceptive Efficacy and, Secondarily, to Assess the Pharmacokinetic Profile and Safety of Two Progestin-only Patches Containing Different Doses of Levonorgestrel (LNG)
Status: Enrolling
Updated:  2/19/2016
Columbia University
mi
from
New York, NY
A Multi-center, Open-label, Randomized, Parallel Group Study to Evaluate Pharmacokinetic Profile, Effects on the Mechanisms of Contraceptive Efficacy and Safety of Two Progestin-only Patches Containing Different Doses of Levonorgestrel (LNG)
CCN009: A Multi-center, Open-label, Randomized, Parallel Group Study to Evaluate the Effects on the Mechanisms of Contraceptive Efficacy and, Secondarily, to Assess the Pharmacokinetic Profile and Safety of Two Progestin-only Patches Containing Different Doses of Levonorgestrel (LNG)
Status: Enrolling
Updated: 2/19/2016
Columbia University
mi
from
New York, NY
Click here to add this to my saved trials
A Multi-center, Open-label, Randomized, Parallel Group Study to Evaluate Pharmacokinetic Profile, Effects on the Mechanisms of Contraceptive Efficacy and Safety of Two Progestin-only Patches Containing Different Doses of Levonorgestrel (LNG)
CCN009: A Multi-center, Open-label, Randomized, Parallel Group Study to Evaluate the Effects on the Mechanisms of Contraceptive Efficacy and, Secondarily, to Assess the Pharmacokinetic Profile and Safety of Two Progestin-only Patches Containing Different Doses of Levonorgestrel (LNG)
Status: Enrolling
Updated:  2/19/2016
University of Cincinnati College of Medicine
mi
from
Cincinnati, OH
A Multi-center, Open-label, Randomized, Parallel Group Study to Evaluate Pharmacokinetic Profile, Effects on the Mechanisms of Contraceptive Efficacy and Safety of Two Progestin-only Patches Containing Different Doses of Levonorgestrel (LNG)
CCN009: A Multi-center, Open-label, Randomized, Parallel Group Study to Evaluate the Effects on the Mechanisms of Contraceptive Efficacy and, Secondarily, to Assess the Pharmacokinetic Profile and Safety of Two Progestin-only Patches Containing Different Doses of Levonorgestrel (LNG)
Status: Enrolling
Updated: 2/19/2016
University of Cincinnati College of Medicine
mi
from
Cincinnati, OH
Click here to add this to my saved trials
A Multi-center, Open-label, Randomized, Parallel Group Study to Evaluate Pharmacokinetic Profile, Effects on the Mechanisms of Contraceptive Efficacy and Safety of Two Progestin-only Patches Containing Different Doses of Levonorgestrel (LNG)
CCN009: A Multi-center, Open-label, Randomized, Parallel Group Study to Evaluate the Effects on the Mechanisms of Contraceptive Efficacy and, Secondarily, to Assess the Pharmacokinetic Profile and Safety of Two Progestin-only Patches Containing Different Doses of Levonorgestrel (LNG)
Status: Enrolling
Updated:  2/19/2016
Magee-Womens Hospital
mi
from
Pittsburgh, PA
A Multi-center, Open-label, Randomized, Parallel Group Study to Evaluate Pharmacokinetic Profile, Effects on the Mechanisms of Contraceptive Efficacy and Safety of Two Progestin-only Patches Containing Different Doses of Levonorgestrel (LNG)
CCN009: A Multi-center, Open-label, Randomized, Parallel Group Study to Evaluate the Effects on the Mechanisms of Contraceptive Efficacy and, Secondarily, to Assess the Pharmacokinetic Profile and Safety of Two Progestin-only Patches Containing Different Doses of Levonorgestrel (LNG)
Status: Enrolling
Updated: 2/19/2016
Magee-Womens Hospital
mi
from
Pittsburgh, PA
Click here to add this to my saved trials
A Multi-center, Open-label, Randomized, Parallel Group Study to Evaluate Pharmacokinetic Profile, Effects on the Mechanisms of Contraceptive Efficacy and Safety of Two Progestin-only Patches Containing Different Doses of Levonorgestrel (LNG)
CCN009: A Multi-center, Open-label, Randomized, Parallel Group Study to Evaluate the Effects on the Mechanisms of Contraceptive Efficacy and, Secondarily, to Assess the Pharmacokinetic Profile and Safety of Two Progestin-only Patches Containing Different Doses of Levonorgestrel (LNG)
Status: Enrolling
Updated:  2/19/2016
Oregon Health and Sciences University
mi
from
Portland, OR
A Multi-center, Open-label, Randomized, Parallel Group Study to Evaluate Pharmacokinetic Profile, Effects on the Mechanisms of Contraceptive Efficacy and Safety of Two Progestin-only Patches Containing Different Doses of Levonorgestrel (LNG)
CCN009: A Multi-center, Open-label, Randomized, Parallel Group Study to Evaluate the Effects on the Mechanisms of Contraceptive Efficacy and, Secondarily, to Assess the Pharmacokinetic Profile and Safety of Two Progestin-only Patches Containing Different Doses of Levonorgestrel (LNG)
Status: Enrolling
Updated: 2/19/2016
Oregon Health and Sciences University
mi
from
Portland, OR
Click here to add this to my saved trials
A Multi-center, Open-label, Randomized, Parallel Group Study to Evaluate Pharmacokinetic Profile, Effects on the Mechanisms of Contraceptive Efficacy and Safety of Two Progestin-only Patches Containing Different Doses of Levonorgestrel (LNG)
CCN009: A Multi-center, Open-label, Randomized, Parallel Group Study to Evaluate the Effects on the Mechanisms of Contraceptive Efficacy and, Secondarily, to Assess the Pharmacokinetic Profile and Safety of Two Progestin-only Patches Containing Different Doses of Levonorgestrel (LNG)
Status: Enrolling
Updated:  2/19/2016
The University of Pennsylvania Medical Center
mi
from
Philadelphia, PA
A Multi-center, Open-label, Randomized, Parallel Group Study to Evaluate Pharmacokinetic Profile, Effects on the Mechanisms of Contraceptive Efficacy and Safety of Two Progestin-only Patches Containing Different Doses of Levonorgestrel (LNG)
CCN009: A Multi-center, Open-label, Randomized, Parallel Group Study to Evaluate the Effects on the Mechanisms of Contraceptive Efficacy and, Secondarily, to Assess the Pharmacokinetic Profile and Safety of Two Progestin-only Patches Containing Different Doses of Levonorgestrel (LNG)
Status: Enrolling
Updated: 2/19/2016
The University of Pennsylvania Medical Center
mi
from
Philadelphia, PA
Click here to add this to my saved trials
A Multicenter, Open-Label, Non-Comparative Study of the Safety and Contraceptive Efficacy of the Woman's Condom
A Multicenter, Open-Label, Non-Comparative Study of the Safety and Contraceptive Efficacy of the Woman's Condom
Status: Enrolling
Updated:  2/19/2016
California Family Health Council
mi
from
Los Angeles, CA
A Multicenter, Open-Label, Non-Comparative Study of the Safety and Contraceptive Efficacy of the Woman's Condom
A Multicenter, Open-Label, Non-Comparative Study of the Safety and Contraceptive Efficacy of the Woman's Condom
Status: Enrolling
Updated: 2/19/2016
California Family Health Council
mi
from
Los Angeles, CA
Click here to add this to my saved trials
A Multicenter, Open-Label, Non-Comparative Study of the Safety and Contraceptive Efficacy of the Woman's Condom
A Multicenter, Open-Label, Non-Comparative Study of the Safety and Contraceptive Efficacy of the Woman's Condom
Status: Enrolling
Updated:  2/19/2016
Magee-Womens Hospital
mi
from
Pittsburgh, PA
A Multicenter, Open-Label, Non-Comparative Study of the Safety and Contraceptive Efficacy of the Woman's Condom
A Multicenter, Open-Label, Non-Comparative Study of the Safety and Contraceptive Efficacy of the Woman's Condom
Status: Enrolling
Updated: 2/19/2016
Magee-Womens Hospital
mi
from
Pittsburgh, PA
Click here to add this to my saved trials
A Multicenter, Open-Label, Non-Comparative Study of the Safety and Contraceptive Efficacy of the Woman's Condom
A Multicenter, Open-Label, Non-Comparative Study of the Safety and Contraceptive Efficacy of the Woman's Condom
Status: Enrolling
Updated:  2/19/2016
Jones Institute of Reproductive Medicine
mi
from
Norfolk, VA
A Multicenter, Open-Label, Non-Comparative Study of the Safety and Contraceptive Efficacy of the Woman's Condom
A Multicenter, Open-Label, Non-Comparative Study of the Safety and Contraceptive Efficacy of the Woman's Condom
Status: Enrolling
Updated: 2/19/2016
Jones Institute of Reproductive Medicine
mi
from
Norfolk, VA
Click here to add this to my saved trials
A Multicenter, Open-Label, Non-Comparative Study of the Safety and Contraceptive Efficacy of the Woman's Condom
A Multicenter, Open-Label, Non-Comparative Study of the Safety and Contraceptive Efficacy of the Woman's Condom
Status: Enrolling
Updated:  2/19/2016
Johns Hopkins Bayview Medical Center
mi
from
Baltimore, MD
A Multicenter, Open-Label, Non-Comparative Study of the Safety and Contraceptive Efficacy of the Woman's Condom
A Multicenter, Open-Label, Non-Comparative Study of the Safety and Contraceptive Efficacy of the Woman's Condom
Status: Enrolling
Updated: 2/19/2016
Johns Hopkins Bayview Medical Center
mi
from
Baltimore, MD
Click here to add this to my saved trials
A Multicenter, Open-Label, Non-Comparative Study of the Safety and Contraceptive Efficacy of the Woman's Condom
A Multicenter, Open-Label, Non-Comparative Study of the Safety and Contraceptive Efficacy of the Woman's Condom
Status: Enrolling
Updated:  2/19/2016
NYU Medical Center Family Planning
mi
from
New York, NY
A Multicenter, Open-Label, Non-Comparative Study of the Safety and Contraceptive Efficacy of the Woman's Condom
A Multicenter, Open-Label, Non-Comparative Study of the Safety and Contraceptive Efficacy of the Woman's Condom
Status: Enrolling
Updated: 2/19/2016
NYU Medical Center Family Planning
mi
from
New York, NY
Click here to add this to my saved trials
A Multicenter, Open-Label, Non-Comparative Study of the Safety and Contraceptive Efficacy of the Woman's Condom
A Multicenter, Open-Label, Non-Comparative Study of the Safety and Contraceptive Efficacy of the Woman's Condom
Status: Enrolling
Updated:  2/19/2016
Columbia University
mi
from
New York, NY
A Multicenter, Open-Label, Non-Comparative Study of the Safety and Contraceptive Efficacy of the Woman's Condom
A Multicenter, Open-Label, Non-Comparative Study of the Safety and Contraceptive Efficacy of the Woman's Condom
Status: Enrolling
Updated: 2/19/2016
Columbia University
mi
from
New York, NY
Click here to add this to my saved trials
A Multicenter, Open-Label, Non-Comparative Study of the Safety and Contraceptive Efficacy of the Woman's Condom
A Multicenter, Open-Label, Non-Comparative Study of the Safety and Contraceptive Efficacy of the Woman's Condom
Status: Enrolling
Updated:  2/19/2016
University of Cininnati College of Medicine
mi
from
Cincinnati, OH
A Multicenter, Open-Label, Non-Comparative Study of the Safety and Contraceptive Efficacy of the Woman's Condom
A Multicenter, Open-Label, Non-Comparative Study of the Safety and Contraceptive Efficacy of the Woman's Condom
Status: Enrolling
Updated: 2/19/2016
University of Cininnati College of Medicine
mi
from
Cincinnati, OH
Click here to add this to my saved trials
A Multicenter, Open-Label, Non-Comparative Study of the Safety and Contraceptive Efficacy of the Woman's Condom
A Multicenter, Open-Label, Non-Comparative Study of the Safety and Contraceptive Efficacy of the Woman's Condom
Status: Enrolling
Updated:  2/19/2016
Oregon Health Scieces University
mi
from
Portland, OR
A Multicenter, Open-Label, Non-Comparative Study of the Safety and Contraceptive Efficacy of the Woman's Condom
A Multicenter, Open-Label, Non-Comparative Study of the Safety and Contraceptive Efficacy of the Woman's Condom
Status: Enrolling
Updated: 2/19/2016
Oregon Health Scieces University
mi
from
Portland, OR
Click here to add this to my saved trials
A Multicenter, Open-Label, Non-Comparative Study of the Safety and Contraceptive Efficacy of the Woman's Condom
A Multicenter, Open-Label, Non-Comparative Study of the Safety and Contraceptive Efficacy of the Woman's Condom
Status: Enrolling
Updated:  2/19/2016
The University of Pennsylvania Medical Center
mi
from
Philadelphia, PA
A Multicenter, Open-Label, Non-Comparative Study of the Safety and Contraceptive Efficacy of the Woman's Condom
A Multicenter, Open-Label, Non-Comparative Study of the Safety and Contraceptive Efficacy of the Woman's Condom
Status: Enrolling
Updated: 2/19/2016
The University of Pennsylvania Medical Center
mi
from
Philadelphia, PA
Click here to add this to my saved trials
A Multicenter, Open-Label, Non-Comparative Study of the Safety and Contraceptive Efficacy of the Woman's Condom
A Multicenter, Open-Label, Non-Comparative Study of the Safety and Contraceptive Efficacy of the Woman's Condom
Status: Enrolling
Updated:  2/19/2016
UT Southwestern Medical Center - Dept. of OB/GYN
mi
from
Dallas, TX
A Multicenter, Open-Label, Non-Comparative Study of the Safety and Contraceptive Efficacy of the Woman's Condom
A Multicenter, Open-Label, Non-Comparative Study of the Safety and Contraceptive Efficacy of the Woman's Condom
Status: Enrolling
Updated: 2/19/2016
UT Southwestern Medical Center - Dept. of OB/GYN
mi
from
Dallas, TX
Click here to add this to my saved trials
Study of Immediate Start of Progestin Contraceptives in Medical Abortion
Immediate Initiation of Progestin Contraceptives in First Trimester Medical Abortion: A Randomized Controlled Trial
Status: Enrolling
Updated:  3/3/2016
Planned Parenthood of the Pacific Southwest
mi
from
Chula Vista, CA
Study of Immediate Start of Progestin Contraceptives in Medical Abortion
Immediate Initiation of Progestin Contraceptives in First Trimester Medical Abortion: A Randomized Controlled Trial
Status: Enrolling
Updated: 3/3/2016
Planned Parenthood of the Pacific Southwest
mi
from
Chula Vista, CA
Click here to add this to my saved trials
Study of Immediate Start of Progestin Contraceptives in Medical Abortion
Immediate Initiation of Progestin Contraceptives in First Trimester Medical Abortion: A Randomized Controlled Trial
Status: Enrolling
Updated:  3/3/2016
Planned Parenthood Northern California
mi
from
Eureka, CA
Study of Immediate Start of Progestin Contraceptives in Medical Abortion
Immediate Initiation of Progestin Contraceptives in First Trimester Medical Abortion: A Randomized Controlled Trial
Status: Enrolling
Updated: 3/3/2016
Planned Parenthood Northern California
mi
from
Eureka, CA
Click here to add this to my saved trials
Study of Immediate Start of Progestin Contraceptives in Medical Abortion
Immediate Initiation of Progestin Contraceptives in First Trimester Medical Abortion: A Randomized Controlled Trial
Status: Enrolling
Updated:  3/3/2016
Planned Parenthood of Southern New England
mi
from
Stamford, CT
Study of Immediate Start of Progestin Contraceptives in Medical Abortion
Immediate Initiation of Progestin Contraceptives in First Trimester Medical Abortion: A Randomized Controlled Trial
Status: Enrolling
Updated: 3/3/2016
Planned Parenthood of Southern New England
mi
from
Stamford, CT
Click here to add this to my saved trials
Study of Immediate Start of Progestin Contraceptives in Medical Abortion
Immediate Initiation of Progestin Contraceptives in First Trimester Medical Abortion: A Randomized Controlled Trial
Status: Enrolling
Updated:  3/3/2016
Bayview Medical Center
mi
from
Baltimore, MD
Study of Immediate Start of Progestin Contraceptives in Medical Abortion
Immediate Initiation of Progestin Contraceptives in First Trimester Medical Abortion: A Randomized Controlled Trial
Status: Enrolling
Updated: 3/3/2016
Bayview Medical Center
mi
from
Baltimore, MD
Click here to add this to my saved trials
Study of Immediate Start of Progestin Contraceptives in Medical Abortion
Immediate Initiation of Progestin Contraceptives in First Trimester Medical Abortion: A Randomized Controlled Trial
Status: Enrolling
Updated:  3/3/2016
Planned Parenthood League of Massachusetts
mi
from
Boston, MA
Study of Immediate Start of Progestin Contraceptives in Medical Abortion
Immediate Initiation of Progestin Contraceptives in First Trimester Medical Abortion: A Randomized Controlled Trial
Status: Enrolling
Updated: 3/3/2016
Planned Parenthood League of Massachusetts
mi
from
Boston, MA
Click here to add this to my saved trials
Study of Immediate Start of Progestin Contraceptives in Medical Abortion
Immediate Initiation of Progestin Contraceptives in First Trimester Medical Abortion: A Randomized Controlled Trial
Status: Enrolling
Updated:  3/3/2016
Boston Med Ctr
mi
from
Boston, MA
Study of Immediate Start of Progestin Contraceptives in Medical Abortion
Immediate Initiation of Progestin Contraceptives in First Trimester Medical Abortion: A Randomized Controlled Trial
Status: Enrolling
Updated: 3/3/2016
Boston Med Ctr
mi
from
Boston, MA
Click here to add this to my saved trials
Study of Immediate Start of Progestin Contraceptives in Medical Abortion
Immediate Initiation of Progestin Contraceptives in First Trimester Medical Abortion: A Randomized Controlled Trial
Status: Enrolling
Updated:  3/3/2016
Centro de Salud Beatriz Velasco de Aleman
mi
from
Mexico City,
Study of Immediate Start of Progestin Contraceptives in Medical Abortion
Immediate Initiation of Progestin Contraceptives in First Trimester Medical Abortion: A Randomized Controlled Trial
Status: Enrolling
Updated: 3/3/2016
Centro de Salud Beatriz Velasco de Aleman
mi
from
Mexico City,
Click here to add this to my saved trials
Postplacental Intrauterine Device Insertion: A Mixed Methods Assessment of Women's Experience
Postplacental Intrauterine Device Insertion: A Mixed Methods Assessment of Women's Experience
Status: Enrolling
Updated:  3/3/2016
University of New Mexico Health Sciences Center
mi
from
Albuquerque, NM
Postplacental Intrauterine Device Insertion: A Mixed Methods Assessment of Women's Experience
Postplacental Intrauterine Device Insertion: A Mixed Methods Assessment of Women's Experience
Status: Enrolling
Updated: 3/3/2016
University of New Mexico Health Sciences Center
mi
from
Albuquerque, NM
Click here to add this to my saved trials
A Safety Study Of The Caya® Diaphragm Used With ContraGel®
A Phase I Safety Study Of The Caya® Diaphragm Used With ContraGel®
Status: Enrolling
Updated:  5/26/2016
Eastern Virginia Medical School
mi
from
Norfolk, VA
A Safety Study Of The Caya® Diaphragm Used With ContraGel®
A Phase I Safety Study Of The Caya® Diaphragm Used With ContraGel®
Status: Enrolling
Updated: 5/26/2016
Eastern Virginia Medical School
mi
from
Norfolk, VA
Click here to add this to my saved trials
PK Patch 12 Week Continuous Use
The Pharmacokinetics of 12 Week Continuous Patch Use
Status: Enrolling
Updated:  6/13/2016
Boston Med Ctr
mi
from
Boston, MA
PK Patch 12 Week Continuous Use
The Pharmacokinetics of 12 Week Continuous Patch Use
Status: Enrolling
Updated: 6/13/2016
Boston Med Ctr
mi
from
Boston, MA
Click here to add this to my saved trials
Retrospective Claims Analysis of Hysterectomy After Sterilization
A Retrospective Claims Analysis to Calculate the Proportion of Women Undergoing Hysterectomy, Salpingectomy, Salpingostomy, Hysteroscopy or Who Had a Diagnosis of Pelvic Pain After Hysteroscopic Sterilization or Laparoscopic Tubal Ligation
Status: Enrolling
Updated:  3/20/2017
mi
from
Whippany, NJ
Retrospective Claims Analysis of Hysterectomy After Sterilization
A Retrospective Claims Analysis to Calculate the Proportion of Women Undergoing Hysterectomy, Salpingectomy, Salpingostomy, Hysteroscopy or Who Had a Diagnosis of Pelvic Pain After Hysteroscopic Sterilization or Laparoscopic Tubal Ligation
Status: Enrolling
Updated: 3/20/2017
mi
from
Whippany, NJ
Click here to add this to my saved trials
Contraceptive Choice at the Time of Uterine Evacuation
Contraceptive Choice at the Time of Uterine Evacuation: A Randomized Controlled Pre-visit LARC Educational Intervention
Status: Enrolling
Updated:  4/17/2017
Planned Parenthood League of Massachusetts
mi
from
Boston, MA
Contraceptive Choice at the Time of Uterine Evacuation
Contraceptive Choice at the Time of Uterine Evacuation: A Randomized Controlled Pre-visit LARC Educational Intervention
Status: Enrolling
Updated: 4/17/2017
Planned Parenthood League of Massachusetts
mi
from
Boston, MA
Click here to add this to my saved trials
Depo Provera Self-Administration Study: Putting a Patient-Centered Practice to the Test at Planned Parenthood
Depo Provera Self-Administration Study: Putting a Patient-Centered Practice to the Test at Planned Parenthood
Status: Enrolling
Updated:  5/1/2017
Planned Parenthood of Central and Greater Northern New Jersey
mi
from
Morristown, NJ
Depo Provera Self-Administration Study: Putting a Patient-Centered Practice to the Test at Planned Parenthood
Depo Provera Self-Administration Study: Putting a Patient-Centered Practice to the Test at Planned Parenthood
Status: Enrolling
Updated: 5/1/2017
Planned Parenthood of Central and Greater Northern New Jersey
mi
from
Morristown, NJ
Click here to add this to my saved trials
Depo Provera Self-Administration Study: Putting a Patient-Centered Practice to the Test at Planned Parenthood
Depo Provera Self-Administration Study: Putting a Patient-Centered Practice to the Test at Planned Parenthood
Status: Enrolling
Updated:  5/1/2017
Planned Parenthood Gulf Coast
mi
from
Houston, TX
Depo Provera Self-Administration Study: Putting a Patient-Centered Practice to the Test at Planned Parenthood
Depo Provera Self-Administration Study: Putting a Patient-Centered Practice to the Test at Planned Parenthood
Status: Enrolling
Updated: 5/1/2017
Planned Parenthood Gulf Coast
mi
from
Houston, TX
Click here to add this to my saved trials
Group Versus Individual Contraceptive Counseling for Resettled African Refugee Women
Salt Lake Refugee Women's Health Project-Group Versus Individual Contraceptive Counseling for Resettled African Refugee Women
Status: Enrolling
Updated:  5/16/2017
University Of Utah Hospital
mi
from
Salt Lake City, UT
Group Versus Individual Contraceptive Counseling for Resettled African Refugee Women
Salt Lake Refugee Women's Health Project-Group Versus Individual Contraceptive Counseling for Resettled African Refugee Women
Status: Enrolling
Updated: 5/16/2017
University Of Utah Hospital
mi
from
Salt Lake City, UT
Click here to add this to my saved trials