study of Oxytocin versus Carbetocin for the prevention of primary post partum hemorrhage following caesarean delivery in pregnant wome
Phase 2
- Conditions
- Health Condition 1: O80-O82- Encounter for delivery
- Registration Number
- CTRI/2024/04/065815
- Lead Sponsor
- self
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
female with singleton, fullterm pregnancy undergoing elective or emergency caesarean section,
Exclusion Criteria
Hypersensitivity to study drugs,
Cases of coagulopathy,uterine fibroid,suspected placental pathology,
Medical diseases such as hypertension,diabetes mellitus,Cardiac ,renal,liver disorders .
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Evaluation of hemodynamic effects of carbetocin in terms of blood loss.Timepoint: 24 hours after ceserean section
- Secondary Outcome Measures
Name Time Method 1.Need of additional uterotonics <br/ ><br>2.Need of blood transfusion to compensate the blood loss. <br/ ><br>3.The adverse effects encountered by the participants.Timepoint: 24 hours after ceserean section