Clinical trials: Postpartum Contraception
Postpartum Health, Breastfeeding
Navigating New Motherhood 2
The primary aim of this study is to determine whether implementation of a postpartum patient navigation program improves health outcomes among low-income women.
- Conditions
- Postpartum Health, Breastfeeding, Contraception, Preventive Care / Anticipatory Guidance
- Trial name
- NNM2 (NCT03922334)
- Testing
- Patient Navigation Program
- Where
- United States
- Volunteers
- 405 people, healthy volunteers welcome
- Sponsor
- Northwestern University
Contraception
Patient Compliance With Long-Acting Reversible Contraception Administration
This a randomized control trial to identify if patients who desire LARC are more likely to have success receiving the desired form of contraception if it is placed a) during the postpartum hospital stay, either in the immediate…
- Trial name
- NCT03305081
- Testing
- Levonorgestrel IUD, copper IUD, etonorgestrel implant
- Where
- United States
- Volunteers
- 45 people, healthy volunteers welcome
- Sponsor
- Tulane University School of Medicine
Post Partum
Advance Supply of Emergency Contraception Compared to Routine Postpartum Care in Teens
This is a pilot randomized controlled trial to assess the effects of advanced supply of emergency contraception versus routine care in a teen postpartum population.
- Trial name
- NCT00433004
- Testing
- Plan B (Levonorgestrel)
- Where
- United States
- Volunteers
- 50 people, healthy volunteers welcome
- Sponsor
- University of Pennsylvania
Contraception
Improving Adherence to Postpartum Family Planning Guidance in Ghana
Evaluating a Postpartum Family Planning Package (PPFP) in a Hybrid Type II implementation study with a stepped-wedge design.
- Trial name
- NCT04306029
- Testing
- Postpartum Family Planning Package
- Where
- 3 sites in Ghana
- Volunteers
- 2,142 people
- Sponsor
- University of Pennsylvania
Postpartum Contraception, Reproductive Health
Predictors of PPIUCD Discontinuation at Two Years: A Clinical Study in Pakistan
This prospective cohort study evaluated the continuation rates, complications, and satisfaction associated with postpartum intrauterine contraceptive devices (PPIUCDs) as a long-acting reversible contraception (LARC) method.
- Conditions
- Postpartum Contraception, Reproductive Health, Family Planning
- Trial name
- NCT06766396
- Testing
- Postpartum Intrauterine Contraceptive Device (PPIUCD).
- Where
- Pakistan
- Volunteers
- 3,400 people, healthy volunteers welcome
- Sponsor
- Services Institute of Medical Sciences, Pakistan
Contraceptive Usage
Immediate Versus Delayed Insertion of Implanon in Postpartum Adolescents
The specific aim of this study is to evaluate whether insertion of a long-acting contraceptive implant in postpartum adolescents prior to hospital discharge increases use of this highly effective contraception during the first…
- Trial name
- Implanon (NCT03585504)
- Testing
- Etonogestrel contraceptive implant
- Where
- United States
- Volunteers
- 81 people, healthy volunteers welcome
- Sponsor
- Medical University of South Carolina
Contraception, Contraceptive Usage
Advance Provision of Postpartum Emergency Contraception and Its Effects on Reproductive Autonomy
This study will entail provision of ulipristal acetate (UPA) for emergency contraception (EC) in the postpartum period for patients who have not chosen to initiate a highly effective form of contraception and study the use of EC…
- Conditions
- Contraception, Contraceptive Usage, Reproductive Issues
- Trial name
- NCT05285605
- Testing
- Ulipristal Acetate
- Where
- United States
- Volunteers
- 75 people
- Sponsor
- Northwestern University
Health Knowledge, Attitudes, Practice
Operations Research to Address Unmet Need for Contraception in the Postpartum Period in Sylhet District, Bangladesh
The proposed operations research study is designed to evaluate a package of family planning services and related behavior change interventions aimed at addressing the unmet need for family planning in postpartum women, integrated…
- Trial name
- NCT01702402
- Testing
- Educational and Behavior Change intervention, Comparison Group
- Volunteers
- 6,916 people
- Sponsor
- Johns Hopkins Bloomberg School of Public Health
Postpartum Family Planning
Impact Evaluation of a Targeted mHealth Intervention to Improve Uptake of Postpartum Contraception in Kenya
The goal of this study is to explore approaches to improve postpartum contraceptive counseling, information, and uptake through a collaboration between the Harvard Chan School, Rutgers School of Public Health, Jacaranda Health…
- Trial name
- NCT06266780
- Testing
- PROMPTS Enhanced Family Planning Counselling
- Where
- Kenya
- Volunteers
- 4,190 people, healthy volunteers welcome
- Sponsor
- Jacaranda Health