Effects of vitamin E and low-dose aspirin, alone or in combination, on Norplant-induced prolonged bleeding

Completed

• Conditions: Contraception; Pregnancy and Childbirth

• Registration Number: ISRCTN77665712
• Lead Sponsor: DP/UNFPA/WHO/World Bank - Special Programme of Research, Development and Research Training in Human Reproduction

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2004-04-01
• Last Update Posted: 13 January 2015

Recruitment & Eligibility

• Status: Completed
• Sex: Female
• Target Recruitment: 486

Inclusion Criteria

1. Women aged 18 - 38 years
2. 1 - 6 months post Norplant insertion
3. Non-lactating
4. Experiencing an episode of vaginal bleeding lasting more than 7 days

Exclusion Criteria

Not provided at time of registration

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
ot provided at time of registration

Secondary Outcome Measures

Name	Time	Method
ot provided at time of registration