To compare blood loss after normal delivery with use of oxytocin alone and oxytocin with misoprotol
Phase 2
- Conditions
- Health Condition 1: O720- Third-stage hemorrhage
- Registration Number
- CTRI/2023/10/059156
- Lead Sponsor
- Intramural Jawarharlal Institute of Postgraduate Medical Education and Research
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Pregnant women = 18 years of age
2. Gestational age =37 weeks to 42 weeks
3. Following singleton vaginal delivery
Exclusion Criteria
1. Antepartum haemorrhage
2. Pre-existing bleeding disorders
3. Fever ( >38?C)
4. Acute Gastroenteritis
5. Known hypersensitivity to Oxytocin or Misoprostol
6. Distressed due to labour pains to give informed consent
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method