Status:

COMPLETED

A Study on the Feasibility and Acceptability of Pericoital Levonorgestrel 1.5mg

Lead Sponsor:

Camber Collective

Collaborating Sponsors:

Population Council

Marie Stopes International

Conditions:

Pregnancy Related

Eligibility:

FEMALE

18-49 years

Brief Summary

This study intends to build on the previous research and gather data in an actual use study / patient registry of pericoital LNG 1.5mg to understand women's acceptability of the product along with ass...

Detailed Description

The study would consist of distributing pericoital LNG 1.5mg across 75 pharmacy sites in Ghana over the course of 12 months. Recruitment will be staggered, and women will be recruited up to 9 months i...

Eligibility Criteria

Inclusion

  • between the age of 18-49 years, is willing to use LNG 1.5 mg tablets as her primary contraceptive method, wants to avoid pregnancy for at least the next 6 months after enrollment, is willing to accept an uncertain risk of pregnancy during the study, and understands that the risk of pregnancy on this method would be slightly higher than other methods of contraception

Exclusion

  • women using one or more of the following contraceptive methods: daily pill, injectable, implant, sterilization

Key Trial Info

Start Date :

October 1 2019

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

November 1 2020

Estimated Enrollment :

1980 Patients enrolled

Trial Details

Trial ID

NCT04058873

Start Date

October 1 2019

End Date

November 1 2020

Last Update

November 5 2021

Active Locations (1)

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Marie Stopes International Ghana

Accra, Ghana

A Study on the Feasibility and Acceptability of Pericoital Levonorgestrel 1.5mg | DecenTrialz