Effects of the copper intrauterine device and injectable progestogen contraceptive on depression and sexual functioning

Not Applicable

• Conditions: Pregnancy and Childbirth; depression,sectual functioning

• Registration Number: PACTR201210000420221
• Lead Sponsor: Effective Care Research Unit

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2012-09-26
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 200

Inclusion Criteria

Women of child bearing age between 18 to 35 years
Women with no evidence of active pelvic infection
Women who have no contraindications to injectable Progestogen or IUD
Women who are prepared to use either method of contraception
Women delivered less than 48 ago.
Women who are willing and able to give consent.

Exclusion Criteria

Recent noticed vaginal bleeding that is unusual.
Any contraindication for deport injection and IUD as stated on the WHO contraceptive eligibility criteria will.
Women at baseline screening with depression score of 29 - 63(severe depression)
Women with no access to telephone

Study & Design

• Study Type: Interventional
• Study Design: Not specified