Comparative long-term effects of depot medroxyprogesterone acetate, a levonorgestrel implant and a copper intrauterine device on depression and sexual

Not Applicable

• Conditions: Mental and Behavioural Disorders; Depression ,sexual dysfunction

• Registration Number: PACTR201801002743482
• Lead Sponsor: Effective Care Research Unit

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2017-11-02
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Pending
• Sex: Female
• Target Recruitment: 291

Inclusion Criteria

¿16 to 35 years of age
¿HIV sero-negative at baseline
¿Seeking effective contraception
¿Able and willing to provide written informed consent
¿Agrees to be randomised to either the copper IUD, DMPA, or LNG implant
¿Agrees to use assigned method for 18 months
¿Agrees to follow all study requirements
¿Intends to stay in the study area for the next 18 months and willing and able to provide adequate locator information
¿If has had a recent third trimester birth, is at least 6 weeks¿ postpartum
¿Is sexually active (has had vaginal sex within the last 3 months) or has been pregnant within the last 3 months
¿Agrees not to participate in studies of drugs or vaccines or any other clinical research study while participating in this study

Exclusion Criteria

Women are not eligible to participate if they have medical contraindications to the IUD, DMPA, or LNG implant (WHO Medical Eligibility Criteria category 3 or 4),

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Depression