TCTR20160715004Completed未知
Efficacy of intravenous 100 mcg carbetocin versus intravenous 5 units oxytocin for prevention of immediate postpartum hemorrhage after normal vagina delivery among high risk prenancies; a tripple-blinded randomized controlled trial
Siriraj Routine to Research Unit0 sites350 target enrollmentStarted: July 15, 2016Last updated:
Conditions
Trial Snapshot
- Phase
- 未知
- Status
- Completed
- Sponsor
- Enrollment
- 350
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
- Ages
- 20 Years to 50 Years (—)
- Sex
- Female
Inclusion Criteria
- •1. Thai pregnant woman
- •2. age at least 20 years old
- •3. Pregnancy age at least 34 weeks gestation
- •4. normal vaginal delvery
- •5. high risk for PPH including previous history of PPH, induction or augmentation of labour, tocolytic drug before delivery, prolonged active phase of labour, precipitate labour, grand multipara, overdistended uterus, uterine structural abnormality
Exclusion Criteria
- •1. being active labour
- •2. Contraindication to carbetocin
- •3. allergy to oxytocin or carbetocin
- •4. obstetrics complication including preeclampsia and abnormal placentation
Investigators
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