跳至主要内容
临床试验/CTRI/2018/02/012173
CTRI/2018/02/012173已完成未知

RANDOMIZED CONTROLLED TRIAL COMPARING EFFICACY OF A COMBINATION REGIME CONTAINING TWO CERVICAL SENSITIZERS (MIFEPRISTONE + FOLEYâ??S CATHETER) VERSUS SINGLE AGENT MIFEPRISTONE OR FOLEYâ??S CATHETER FOR LABOR INDUCTION IN WOMEN ATTEMPTING TOLAC AT LATE THIRD TRIMESTER WITH A DEAD FETUS IN UTERO

Department of Obstetrics and Gynaecology Chittaranjan Seva Sadan and Shishu Sadan0 个研究点目标入组 192 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
已完成
发起方
入组人数
192

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • Women of age 20 years and above, with a history of previous cesarean birth, singleton pregnancy, IUFD diagnosed at a gestational age of 34 weeks or above and with bishop score (BS) <= 6 were eligible for recruitment.

排除标准

  • Women with known allergy/contraindication to the use of mifepristone, previous two or more caesarean births (or myomectomy), evidence of coagulopathy, serious medical complications, low-lying placenta, clinical suspicion of chorioamnionitis, any systemic infection at the time of examination and multi-parity (parity > four) were excluded.

研究者

发起方
Department of Obstetrics and Gynaecology Chittaranjan Seva Sadan and Shishu Sadan

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