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Pregnancy Prevention clinical trials

View clinical trials related to Pregnancy Prevention.

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NCT ID: NCT05360576 Completed - Clinical trials for Pregnancy Prevention

An Open-label, Randomized, 2-Period, Crossover, Pharmacokinetics Study

Start date: February 24, 2022
Phase: Phase 2
Study type: Interventional

An Open-label, Randomized, 2-Period, Crossover Study to Assess the Comparative Pharmacokinetics of LSP-5415 and NuvaRing® in Healthy Adult Females

NCT ID: NCT05360550 Completed - Clinical trials for Pregnancy Prevention

A Study to Evaluate the Effect of a Contraceptive Vaginal Ring LSP- 5415 on Ovarian Function in Healthy Adult Females

Start date: July 5, 2022
Phase: Phase 2
Study type: Interventional

The primary objective of this study is to evaluate the inhibition of ovulation in Cohort #1 (Body Mass Index of ≥ 18 kg/m2 to ≤ 30 kg/m2) after contraceptive vaginal ring LSP-5415 application for 3 treatment cycles.

NCT ID: NCT04233632 Completed - Clinical trials for Pregnancy Prevention

Comparative Study of the Contraceptive Efficacy of the Cupid, Cupid 2 and FC2 Female Condom

Start date: November 27, 2019
Phase: N/A
Study type: Interventional

This research study aims to assess the effectiveness of three female condoms [Cupid, Cupid 2 and Female Condom 2(FC2)] for the prevention of pregnancy among women choosing the female condom (FC) as their method of fertility regulation. Participants will be followed-up monthly for up to seven months. A daily diary will be used to record menstrual pattern, acts of intercourse and details of condom usage.

NCT ID: NCT04076774 Completed - HIV Prevention Clinical Trials

A Functional Performance Study of The Wondaleaf Female Condom

Start date: March 27, 2019
Phase: N/A
Study type: Interventional

This research study will determine how well two female condoms perform when used during sex. One of these condoms (FC2) is already commercially available in South Africa. The other female condom, "Wondaleaf Condom" is a new female condom. Participants will use both condoms. The study aims to determine how well these condoms work comparatively. Study visits include a screening/enrolment visit and 2 follow up visits.

NCT ID: NCT03366636 Completed - Clinical trials for Sexually Transmitted Diseases

Project Legacy Impact Evaluation Study

Start date: October 30, 2017
Phase: N/A
Study type: Interventional

This study will design and rigorously evaluate the efficacy of Project Legacy, a five week positive youth development intervention to decrease sexual risk for unintended pregnancies and STIs among youth experiencing homelessness or at risk of homelessness aged 14-19. This randomized control trial will compare Project Legacy to a usual services control.

NCT ID: NCT03194672 Completed - Clinical trials for Pregnancy Prevention

Healthy Adolescent Transitions (HAT)

HAT
Start date: August 14, 2017
Phase: Phase 2
Study type: Interventional

Randomized trial of a rapid repeat pregnancy prevention program for adolescent mothers. Five hundred adolescent mothers from central Ohio will be enrolled--half will be assigned to an intervention that features nurses and social workers providing extra assistance during late pregnancy and the early postnatal period and half will be assigned to a standard of care intervention. OhioHealth is the lead entity. Nationwide Children's Hospital serves as the local independent evaluator. This federally funded contract is supported by the Family and Youth Services Bureau.

NCT ID: NCT03063385 Completed - Clinical trials for Sexually Transmitted Diseases

Puerto Rico Cuidalos Parent-adolescent Program

Start date: September 2012
Phase: N/A
Study type: Interventional

Latino adolescents are at high risk for HIV/AIDS, other sexually transmitted infections (STIs), and unintended pregnancies. Puerto Rican adolescents, in particular, experience disparities in these areas, yet few adolescent and even fewer parent interventions have been developed to address these important issues with this underserved population. Parent-adolescent programs are an effective approach to reduce adolescent sexual risk behavior and associated negative consequences. A web-based parent communication intervention provides an opportunity to strengthen and enhance programs that are designed for adolescents by providing additional support for safer sex decisions, and to increase parents' access to sexual health education programs by decreasing barriers that keep them from participating in these interventions (e.g., low cost, can be viewed privately, at parents convenience, minimizes competing time with work and family). The purpose of this proposed study is to evaluate a brief theoretically informed (i.e., Ecodevelopmental Theory, Theory of Reasoned Action/Planned Behavior, Social Cognitive Theory 1-6), culturally appropriate, and linguistically tailored web-based parental communication program, Cuídalos ("Take care of them"), designed to improve parent-adolescent sexual communication and reduce adolescent sexual risk behavior. Recent findings from an NIH funded R21 randomized control trial (RCT) testing a brief computer-based version of the Cuídalos program indicated that the program increased parent-adolescent general communication and sexual risk communication with English and Spanish speaking U.S. Latinos. Further, despite limited or no previous computer use, parents reported they liked and learned from the program, and that it was easy to use and accessible.

NCT ID: NCT01535651 Completed - Clinical trials for Pregnancy Prevention

Using Social Media to Enhance the Impact of the Teen Outreach Program

TOP4ME
Start date: September 2011
Phase: N/A
Study type: Interventional

The investigators are exploring the use of short message service (text) messaging by cell phones to enhance the effects of the Teen Outreach Program, an effective teen pregnancy prevention program.

NCT ID: NCT00996580 Completed - Clinical trials for Pregnancy Prevention

A Study to Evaluate the Efficacy and Safety of DR-103 for the Prevention of Pregnancy

Start date: October 2009
Phase: Phase 3
Study type: Interventional

This is an open-label, single-treatment study. All subjects will receive 12 months of oral contraceptive therapy with DR-103. Study participants will receive physical and gynecological exams, including Pap smear. During the study, all participants will be required to complete a diary.

NCT ID: NCT00570440 Completed - Clinical trials for Pregnancy Prevention

Continuous Use of COCs

Start date: August 2007
Phase: Phase 4
Study type: Interventional

The primary objective is to determine if continuous COC use leads to higher continuation rates over 12 months of follow up than use of the standard 28-day COC regimen.