Evaluation of intrauterine balloon tamponade efficacy with condom catheter and misoprostol (usual treatment) compared to misoprostol alone in the severe postpartum management hemorrhage management in Benin and Mali: a randomized controlled trial

Institute of Research for Development (Institut de Recherche pour le Développement) (IRD)0 个研究点目标入组 110 人开始时间: 2013年9月9日最近更新: 2017年3月13日

试验速览

暂无简介。

•1. Having given birth by vaginal way, in one of the selected establishments
•2. After 28 weeks of amenorrhea, or foetus > 1000 g
•3. Presenting a HPPI resisting the oxytocine and the first-line laborers (uterine massage + uterine revision)
•4. Having given its oral consent

•1. Having given birth by caesarian
•2. Presenting a contraindication or an allergy known about prostaglandins
•3. Presenting an allergy to latex
•4. Presenting a clinical Chorioamnionitis
•5. Presenting a secondary postpartum hemorrhage, cervico-vaginal tears without uterine bleeding, an uterine break, or a placenta accreta

发起方

Institute of Research for Development (Institut de Recherche pour le Développement) (IRD)