Success of intrauterine contraceptive device retention just after the delivery
Not Applicable
- Conditions
- Contraception
- Registration Number
- SLCTR/2014/022
- Lead Sponsor
- District General Hospital, Ampara
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Not specified
- Target Recruitment
- 86
Inclusion Criteria
1. Women with planned vaginal deliveries
2. Desire for copper IUD insertion
Exclusion Criteria
1. Any contraindications for IUD insertion including infection, hemorrhage and caesarian delivery
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Retention of IUD within uterine cavity [At 12 hours of insertion and at 6-8 weeks post partum]<br>
- Secondary Outcome Measures
Name Time Method one [None]<br>