Contraceptive Usage

6

Review clinical trials related to Contraceptive Usage. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Efficacy, Safety, and Tolerability of Levonorgestrel Vaginal System

The goal of this clinical trial is to learn if drug levonorgestrel vaginal ring works as a contraceptive adult and adolescent females who are able to conceive (i.e. get pregnant). It will also learn about the safety and tolerability of levonorgestrel vaginal ring. The main questions it aims to answer are: Does drug levonorgestrel vaginal ring lower the number of pregnancies with continued use? What adverse effects do participants experience by using levonorestrel vaginal ring? Researchers will count the number of pregnancies with levonorgestrel vaginal ring after a participant uses it for a year to see if the number of pregnancies is low (i.e. women and girls do not get pregnant). Participants will: Use levonorgestrel vaginal ring for 28 days (called one cycle); for a total of 14 cycles (which is a little more than year) Visit the clinic about 8 to 10 times over about 14 months for checkups and tests with an additional approximately 13 phone calls Keep a diary of their pregnancies and number of times they use additional contraceptive (e.g. condoms)

Participants needed: 1,600
Trial details
Phase: Phase 3Age: 13-45Biological sex: FemaleType: InterventionalSponsor: Chemo ResearchUpdated: Jul 29, 2026
Eligibility criteria

Female between age 13 and 45 years [+15]

Status: Recruiting

Disparities in Emergency Contraceptive Metabolism Dictate Efficacy

The purpose of this study is to learn more about why some people are at greater risk for oral emergency contraceptive failure while others are not. The investigators want to learn if genetic differences impact the risk of emergency contraception failure.

Participants needed: 140
Trial details
Phase: Phase 4Age: 18-40Biological sex: FemaleType: InterventionalSponsor: Oregon Health and Science UniversityUpdated: Jul 9, 2026Locations: 1
Eligibility criteria

Generally healthy women [+2]

Pregnant, seeking pregnancy, or breastfeeding [+8]

Status: Not yet recruiting

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 Health and HIV Research (CeSHHAR Zimbabwe). The goal of the proposed study is to evaluate the appropriateness, feasibility, acceptability, uptake, costs and cost-effectiveness of a community-based, HIV-status neutral peer-led service delivery model in which young mentor mothers (YMM) work with pregnant and lactating adolescent girls and young women (PL-AGYW, aged 15-24), up to two-years post-birth, in Zimbabwe to promote uptake of contraception and HIV prevention. YMM living with HIV have been found to be effective in supporting their peers for prevention of mother-to-child transmission of HIV and adherence to treatment through the "Zvandiri" programme. The investigators propose adapting the "Zvandiri" YMM to include those without HIV to promote behaviour to prevent HIV and unintended pregnancies. This proposed intervention is building on the formative work that had the overall aim of co-developing with AGYW (aged 15-24) a Pre-Exposure Prophylaxis (PrEP) implementation intervention for AGYW who need it, that attracts them to PrEP, and supports pregnant and lactating adolescent girls and young women while taking it.

Participants needed: 600
Trial details
Age: 15-24Biological sex: FemaleType: InterventionalSponsor: University College, LondonUpdated: Apr 22, 2026Locations: 3
Eligibility criteria

either pregnant or have at least one child who is less than 18 months of age at... [+1]

Status: Recruiting

Effectiveness Testing of a Videogame Intervention (No Baby No) to Decrease Contraception Non-use Among Adolescents.

The purpose of this study is to evaluate the effectiveness of a videogame compared to an attention/time control at reducing contraceptive non-use among adolescents.

Participants needed: 850
Trial details
Age: 15-20Biological sex: AllType: InterventionalSponsor: Weill Medical College of Cornell UniversityUpdated: Dec 22, 2025Locations: 7
Eligibility criteria

Male or Female [+3]

Age less than 15 or older than 20 [+2]

Status: Recruiting

Assess Performance Attributes and Acceptability of Non-medicated Intravaginal Rings Among Sexually Active Women in Atlanta, GA

A randomized open label crossover trial to assess performance attributes and acceptability of non-medicated intravaginal rings among sexually active women in Atlanta, GA

Participants needed: 60
Trial details
Phase: Early Phase 1Age: 18-49Biological sex: FemaleType: InterventionalSponsor: Population CouncilUpdated: Sep 5, 2025Locations: 1
Eligibility criteria

1. Cisgender female aged 18-49 years old, inclusive, at screening based on self-...

1. Known or suspected allergy to silicone or EVA, as reported by participant. 2....

Status: Recruiting

Telemedicine Contraceptive Counselling (TECC) Versus Standard Care

Overall purpose of the PILOT and RCT: This research project aims to increase access and uptake of contraception after abortion through the systematic development and testing of a new telemedicine service for contraceptive counselling (TECC). The investigators will perform a pilot study in South Africa, and multicenter randomized controlled trial in South Africa and Kenya with the following specific aims:

Participants needed: 510
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: Karolinska InstitutetUpdated: Nov 12, 2024Locations: 2
Eligibility criteria

Seeking either surgical or medical abortion [+4]