Clinical trials: Contraception Use
Contraception
Evaluating Household Visits and Small Groups to Increase Contraception Use Among Married Adolescent Girls in Rural Niger
This study entails a quasi-experimental, mixed-methods (i.e., complementary quantitative and qualitative) outcome evaluation to assess the efficacy of the Reaching Married Adolescents (RMA) Interventions developed and implemented…
- Trial name
- IMPACT-RMA (NCT03226730)
- Testing
- Household Visits, Small Groups
- Where
- 2 sites in United States, Niger
- Volunteers
- 2,898 people
- Sponsor
- University of California, San Diego
Contraceptive Behavior
Meaningful Use of Technology to Improve Health Care Delivery
While there have been major declines in teenage pregnancy around the country, Baltimore, Maryland has continued to experience increases over the last several years.
- Trial name
- DepoText (NCT01641380)
- Testing
- Text Messaging Intervention
- Where
- United States
- Volunteers
- 100 people, healthy volunteers welcome
- Sponsor
- Johns Hopkins University
Contraception
I-CAN Uganda Effectiveness Trial
This is a cluster-randomized controlled trial to determine the effectiveness of the community-based "I-CAN" intervention to improve agency in contraceptive decision-making and use in rural Uganda.
- Trial name
- I-CAN (NCT07711717)
- Testing
- I-CAN
- Where
- Uganda
- Volunteers
- 1,560 people
- Sponsor
- University of California, San Francisco
Contraceptive Usage, Coagulation
How DHEA Supplements Affect Coagulation in Women Using Birth Control Pills
A randomized study is to learn more about how a supplement called DHEA (dehydroepiandrosterone) affects clotting factors in women taking combined oral contraceptive pills.
- Trial name
- COC+DHEA (NCT03418363)
- Testing
- DHEA Oral Capsule
- Where
- United States
- Volunteers
- 15 people, healthy volunteers welcome
- Sponsor
- Oregon Health and Science University
Contraceptive Usage, HIV Infections
Effect of Dolutegravir on Etonogestrel Levels in HIV-infected Women in Botswana
The primary aim is to assess if etonogestrel (ENG) implant users taking dolutegravir (DTG) have a 20% or greater change in their ENG plasma levels, compared to women taking no antiretroviral therapy (ART).
- Conditions
- Contraceptive Usage, HIV Infections, Drug Interaction
- Trial name
- NCT03336346
- Testing
- dolutegravir, ENG implant, Efavirenz
- Where
- Botswana
- Volunteers
- 148 people, healthy volunteers welcome
- Sponsor
- Columbia University
HIV Prevention, Contraceptive Usage
Peer-led Service Delivery Model for Pregnant and Lactating Adolescent Girls and Young Women in Zimbabwe
This is a pilot cluster-randomized control trial co-led by Dr. Valentina Cambiano, Associate Professor of Epidemiology at University College London, UK and Professor Euphemia Sibanda, Research Director at the Centre for Sexual…
- Conditions
- HIV Prevention, Contraceptive Usage, Adherence, Medication
- Trial name
- Ontanga (NCT07546344)
- Testing
- Peers who are stars
- Where
- 3 sites in Zimbabwe
- Volunteers
- 600 people, healthy volunteers welcome
- Sponsor
- University College, London
Contraceptive Usage
Ablation of Subcutaneous Contraceptive Implants in the Operating Room
The ablation of subcutaneous contraceptive implants is usually performed in consultation under local anesthesia. However, it happens that the implant was placed too deeply or that it migrated too deeply making it impossible to…
- Trial name
- TAICS (NCT05932537)
- Testing
- Preoperative visualization techniques
- Where
- France
- Volunteers
- 50 people
- Sponsor
- Hospices Civils de Lyon
Contraceptive Behavior
Long Term and Permanent Contraceptive
We will study with the different variables that affect the intention to use long- acting and permanent contraceptive methods among married women in Jordan through a cross sectional study.
- Trial name
- NCT04672304
- Testing
- Al-Husban University Naser
- Where
- Jordan
- Volunteers
- 1,365 people, healthy volunteers welcome
- Sponsor
- University of Jordan
Contraception
Continuous Versus Cyclic Use of Oral Contraceptive Pills in Adolescents
The primary purpose of this study is to compare the compliance rates of adolescents who take oral contraceptives (OCPs) continuously to those who take OCPs cyclically.
- Trial name
- NCT00326404
- Testing
- Desogestrel-Ethinyl Estradiol 21 tablets, Desogestrel-Ethinyl Estradiol 28 tablets
- Where
- Canada
- Volunteers
- 130 people
- Sponsor
- The Hospital for Sick Children
Contraceptive Behavior, Self Administration
Impact of Self-Care Family Planning Services on Health and Development in South Sudan (Family Planning Impact Lab)
Since 2019, the International Rescue Committee (IRC) has led family planning programming under the Women's Integrated Sexual Health (WISH) program, funded by the United Kingdom's Foreign, Commonwealth, and Development Office.
- Trial name
- FPIL (NCT07888296)
- Testing
- Self-Managed Contraceptive Care, Standard Family Planning Services (WISH-2)
- Where
- South Sudan
- Volunteers
- 2,736 people, healthy volunteers welcome
- Sponsor
- Guttmacher Institute
Contraception
Use of Misoprostol for Intrauterine Device (IUD) Insertion in Nulliparous Women
The purpose of this study is to evaluate if the use of misoprostol can make it easier for a provider, and less painful for a woman, to place an IUD if she has never had a child before.
- Trial name
- NCT01001897
- Testing
- Misoprostol
- Where
- 2 sites in United States
- Volunteers
- 61 people, healthy volunteers welcome
- Sponsor
- University of Arizona
Contraception
Evaluation of a Contraceptive Counseling Intervention in Deprived Neighborhoods: SIRIAN Randomized Controlled Trial
This study evaluates the effects of a community-based counseling intervention to improve contraception among residents in two deprived neighborhoods in Barcelona (Spain).
- Trial name
- SIRIAN (NCT02819388)
- Testing
- Contraceptive counseling
- Where
- Spain
- Volunteers
- 500 people, healthy volunteers welcome
- Sponsor
- Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau
Depression, Postpartum, Anxiety, Postpartum
Efficacy of Mother's Time in Ethiopia
Mother's Time is an evidence-based cognitive behavioral therapy (CBT) tool designed to support postpartum women experiencing mild to moderate symptoms of stress, depression or anxiety.
- Conditions
- Depression, Postpartum, Anxiety, Postpartum, Contraceptive Usage
- Trial name
- NCT05806463
- Testing
- Mother's Time
- Where
- Ethiopia
- Volunteers
- 328 people
- Sponsor
- Johns Hopkins Bloomberg School of Public Health
Contraceptive Usage
Increase First-time Mothers' Use of Postpartum Family Planning in Bangladesh: The Connect Project
While a growing body of programs have shown promise to increase uptake of contraception among FTMs, difficulties remain in scaling beyond small pilot areas and institutionalizing within existing systems.
- Trial name
- Connect BD (NCT06666036)
- Testing
- Connect
- Where
- Bangladesh
- Volunteers
- 2,308 people, healthy volunteers welcome
- Sponsor
- George Washington University
Contraception, HIV
Protease Inhibitors and Combined Oral Contraceptive Pharmacokinetics and Pharmacodynamics
The project is a two-arm prospective cohort and pharmacokinetic study comparing levonorgestrel and ethinyl estradiol pharmacokinetics in HIV-positive women taking antiretroviral regimens that include ritonavir to those in women…
- Trial name
- NCT02531321
- Testing
- Levonorgestrel and Ethinyl Estradiol
- Where
- United States
- Volunteers
- 17 people
- Sponsor
- University of Southern California
Emergency Contraception, Contraception
Continued Use of Effective Contraception After Use of Emergency Contraception
Women using an emergency contraceptive method must use back up protection for 1-2 weeks depending on method. The Copper-IUD is the most effective emergency contraceptive method.
- Conditions
- Emergency Contraception, Contraception, Reproductive Health
- Trial name
- NCT02078414
- Where
- Sweden
- Volunteers
- 7 people
- Sponsor
- Karolinska Institutet
Contraception
Nexplanon and Combined Oral Contraceptive (COC) Combined Use Study
Women currently using or starting a combined oral contraceptive will be offered study enrollment. Study subjects will have a Nexplanon placed and followed for 6 months to evaluate if they continue the COC, continue the implant…
- Trial name
- NexTOC (NCT02852265)
- Testing
- Etonogestrel contraceptive implant
- Where
- United States
- Volunteers
- 20 people, healthy volunteers welcome
- Sponsor
- University of California, Davis
Contraception
Assessing Adolescent Use of Nexplanon Over Time
The purpose of this study is to compare Nexplanon decision-making, uptake, satisfaction and contraceptive outcomes (continuation, switching, discontinuation) over a 12-month period among adolescents ages 15-18 to adolescents ages…
- Trial name
- NCT04889079
- Testing
- Contraceptive use (continuation/switching/discontinuation)
- Where
- United States
- Volunteers
- 255 people, healthy volunteers welcome
- Sponsor
- University of Utah
Emergency Contraception
Emergency Contraception Actual Use Study
This is a non-comparative case series study to assess the ability of females 11-16 years of age, inclusive, who are requesting emergency contraception (EC) to use the study product, DR-104 (Plan B® 1.5), appropriately and safely…
- Trial name
- NCT00777556
- Testing
- DR-104
- Where
- 5 sites in United States
- Volunteers
- 343 people, healthy volunteers welcome
- Sponsor
- Duramed Research
Abortion
What is the Knowledge and Use of Emergency Contraception
The main objective is to assess the knowledge of women seeking abortion about emergency contraception. The secondary objectives are to evaluate the use of emergency contraception among women seeking abortion and to identify…
- Trial name
- NCT03688581
- Where
- France
- Volunteers
- 250 people
- Sponsor
- University Hospital, Strasbourg, France