CTRI/2011/05/001770已完成未知
A randomized trial to compare two dosage schedule of misoprostol following mifepristone for midtrimester termination of pregnancy(12-20weeks).
RS Medical CollegeKolkata0 个研究点目标入组 200 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
- 200
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 opting for abortion during 12-20 weeks
排除标准
- •Known hypersensitivity to mifepristone,misoprostol
- •Scarred uterus
- •Low lying placenta
- •Hb less than 8 gm%
- •Serious medical Diseases
- •Features of Inevitable abortion.
研究者
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