CONTRACEPTION WITH COPPER-T IMMEDIATELY FOLLOWING CHILD BIRTH
Not Applicable
- Registration Number
- CTRI/2011/08/001933
- Lead Sponsor
- I
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 30
Inclusion Criteria
females of reproductive age were selected in immediate postpartum period Incidence(i.e. immediately following delivery of placenta, intracaesarean or within 48 hours after delivery of baby)
Exclusion Criteria
prolonged rupture of membrane18 hr
unresolved postpartum haemorrhage
distorted uterus
extensive genital trauma
trophoblastic disease
AIDS
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method non-expulsion of intra-uterine contraceptive deviceTimepoint: patients will be followed up for 3 months after insertion
- Secondary Outcome Measures
Name Time Method oneTimepoint: N/A