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临床试验/IRCT201106213485N3
IRCT201106213485N3已完成2 期

Scientific Title :Comparison the effect of vaginal and sublingual Misoprostol in successful termination of pregnancy in 12-24 weeks pregnant women admitted in Alzahra Hospital – Rasht in 2011-2012

Vice Chancellor for research, Guilan University of Medical Sciences0 个研究点目标入组 268 人开始时间: 待定最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
268

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
15 years 至 45 years(—)
性别
Female

入选标准

  • Inclusion criteria : 12-24 weeks single pregnancy confirmed with certain LMP and > 20 weeks sonography
  • Exclusion criteria : Known sensitivity to prostaglandins (questions such as skin rash, wheels, dyspnea, cough, chest pain, blurred vision); previous caesarian section; Vaginal bleeding; placenta previa; Parity > 3

排除标准

  • 未提供

研究者

发起方
Vice Chancellor for research, Guilan University of Medical Sciences

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