TCTR20190829003CompletedPhase 3
Intravenous plus intramyometrial oxytocin versus intravenous carbetocin during caesarean section in prevention of post-partum hemorrhage: a randomized controlled trial
Conditions
Trial Snapshot
- Phase
- Phase 3
- Status
- Completed
- Enrollment
- 50
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
- Ages
- 18 Years to 55 Years (—)
- Sex
- Female
Inclusion Criteria
- •1. Pregnant women undergo cesarean section with complete inform consent
- •2. Age older than 18 years old
- •3. Patient can able to fully understand Thai language
- •4. No underlying hematologic disease
Exclusion Criteria
- •History drug (oxytocin or carbetocin) allergy
- •Placenta previa totalis
- •Abruptio placenta
- •Maternal illness (cardio,thyroid,preeclampsia, gestational diabetes,lung,liver,renal, anticoagulant)
- •Twin pregnancy
- •Classical uterine incision procedure
- •Fetal distress
Investigators
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