A comparative study of lesser dose of carbetocin versus regular dose of carbetocin in the prevention of bleeding during planned cesarean delivery
Not Applicable
Completed
- Conditions
- Health Condition 1: O721- Other immediate postpartum hemorrhage
- Registration Number
- CTRI/2022/03/041222
- Lead Sponsor
- Dr Rajasri G Yaliwal
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 216
Inclusion Criteria
Consenting Term pregnancy(37-42 weeks of gestation) undergoing elective LSCS under subarachanoid block (Spinal Anesthesia)
Exclusion Criteria
1.Women in labour
2. Women having Coagulopathies
3. Women with Hypertensive disorder
4. Women with cardiaovascular disorders, hepatic and renal diseases
5. Women with Epilepsy
6. Women having known conditions predisposing to atonic PPH like hydramnios, Multiple gestation prolonged labor.
7. Women requiring General Anaesthesia
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Assessment of blood loss: Change in the pre and post hemoglobin levels and hematocritTimepoint: 72 hours after the operation
- Secondary Outcome Measures
Name Time Method cardoivasular changes and tone of the uterusTimepoint: 1 min <br/ ><br>5min <br/ ><br>10min <br/ ><br>15min <br/ ><br>1hour