Comparison between two regimens of a particular drug Oxytocin (used for contraction of uterus) to evaluate Blood loss between them during Cesarean section.
Phase 4
Completed
- Conditions
- Health Condition 1: null- Pregnant patients posted for cesarean section
- Registration Number
- CTRI/2018/04/013519
- Lead Sponsor
- Vardhman Mahavir Medical College and Safdarjung Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 250
Inclusion Criteria
1. pregnant patients posted for LSCS (Elective/Emergency)
2. Age >18yrs
3. Singleton term pregnancy
4. Planned spinal anesthesia
5. Fulfilling ASA I or II criteria
6. Hb>=10 gm%
Exclusion Criteria
1. Placenta previa, PIH
2. Coagulopathies/thrombocytopenia/ on anticoagulants
3. History of previous obstetric hemorrhage
4. Grand multiparity, Fibroid uterus, hydramnios
5. Severe systemic disease
6. Failure of spinal anesthesia/conversion to GA
7. Traumatic hemorrhage during CS
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method