A study to compare CuT insertion immediately after delivery of baby to the traditional interval insertio
Not Applicable
- Registration Number
- CTRI/2020/05/025357
- Lead Sponsor
- Dr Kavita Khoiwal
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Women who are willing for post-placental or interval IUCD insertion and comply with the study protocol
Exclusion Criteria
woman who has any contraindication for post-placental IUCD insertion, like chorioamnionitis, prolonged rupture of membranes >18 hours, puerperal sepsis and unresolved post-postpartum haemorrhage. Woman who has contraindication for interval IUD insertion, namely pregnancy, active genital infection, uncontrolled blood sugar or genital malignancy
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method