A study to compare between preoperative and postoperative misoprostol pushed rectally to control blood loss after cesarean sectio
Phase 3
- Conditions
- Health Condition 1: O72- Postpartum hemorrhage
- Registration Number
- CTRI/2020/10/028736
- Lead Sponsor
- IPGMER
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Pregnant women at term who are electively prepared for caesarean section under regional anaesthesia.
Exclusion Criteria
Antepartum haemorrhage, maternal hypertension, coagulation disorder, previous 2 or more caesarean section, multiple gestation, fetal macrosomia, polyhydramnios, previous uterine rupture, hypersensitivity to prostaglandin.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method