Comparative study on the safety and acceptability of post-delivery intrauterine contraceptive device using standard approach (Forceps) and a new device (Inserter).
Phase 3
Completed
- Registration Number
- CTRI/2016/03/006771
- Lead Sponsor
- SAID
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 500
Inclusion Criteria
Women who request a PPIUCD insertion during ANC period, at the time of delivery or immediately afterwards, as well as meet overall medical eligibility criteria for the immediate PPIUCD services WHO - IUCD Medical
Eligibility Criteria and gives a written and an audio-visual consent as per the protocol.
Exclusion Criteria
Participants with ruptured membranes more than 18 hours prior to delivery.
Diagnosis of chorio-amnionitis at the time of delivery.
Unresolved postpartum hemorrhage.
Beyond 48 hrs postpartum.Undergone caesarean section.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method