IRCT2017040633255N1已完成3 期
Comparison of The effect between two dose (800 µg/day & 400 µg/6) of vaginal misoprostol in the termination of first-trimester pregnancy: a double-blinded randomized trial
vice chancellor for research of Shahid Beheshti University of Medical Sciences0 个研究点目标入组 90 人开始时间: 待定最近更新:
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 发起方
- 入组人数
- 90
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
- 年龄范围
- 12 years 至 no limit（—）
- 性别
- Female
入选标准
- •Inclusion Criteria: singleton pregnancy; indication for pregnancy termination due to either fetal or maternal causes and gestational age lower than 96 days; no previous misoprostol consuming.
- •exclusion criteria: any sign or symptom of threatened; spontaneous abortion before therapy such as bleeding; any degree of dilatation in cervix or uterine regular contractions before drug administration.
排除标准
- 未提供
研究者
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