跳至主要内容
临床试验/IRCT20200122046221N1
IRCT20200122046221N1招募中3 期

Comparison of the efficacy and side effects of oxytocin + misoprostol with methyl ergonovine (metergin) + misoprostol and misoprostol alone in the excretion of pregnancy products.

Jahrom 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
招募中
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
18 years 至 45 years(—)
性别
Female

入选标准

  • tendency toward outpatient treatment
  • gestational age less than 14 week
  • not presence of high risk disease

排除标准

  • presence of a major disease
  • the patients who can not tolerate drugs
  • those who get tired from the process of treatment

研究者

发起方
Jahrom University of Medical Sciences

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