CTRI/2024/02/062831Not yet recruitingPhase 4
A double blinded randomized controlled study to assess safety and effectiveness of carbetocin vs oxytocin during active management of third stage, for prevention of PPH in patients undergoing cesarean section - nil
siddaganga medical college and research institute0 sites0 target enrollmentStarted: TBDLast updated:
Trial Snapshot
- Phase
- Phase 4
- Status
- Not yet recruiting
- Sponsor
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
Inclusion Criteria
- •willing to participate
- •gestational age 36 weeks-41 weeks
- •patients undergoing cesarean section
Exclusion Criteria
- •hypertensive
- •pre eclampsia
- •ante partum hemorrhage
- •bleeding disorders
- •thrombocytopenia
- •blood coagulation abnormalities
- •cardiovascular disorders
- •renal disease
- •liver disease
- •general anesthesia
- •retained placenta
- •placenta accreta
- •placenta previa
- •previous pph
- •grand multipara
- •fibroid with pregnancy
- •prolonged labour
- •hypersensitivity to oxytocin or carbetocin
- •traumatic pph
Investigators
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