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临床试验/IRCT2014050210901N6
IRCT2014050210901N6已完成未知

Comparison of outcomes and complications of vaginal misoprostol Preoperative administration of oxytousin infusion during surgery to reduce bleeding during abdominal myomectomy

Female Reproductive Research Center, Tabriz University of Medical Sciences0 个研究点目标入组 105 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
105

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
no limit 至 no limit(—)
性别
Female

入选标准

  • the desire to participate in the study

排除标准

  • allergy to misoprostol or oxytocin; hormone therapy before surgery or gonadotropin releasing drugs such as oral contraceptive pills; active liver disorders - kidney disease - heart - lung ; candidates hysteroscopic myomectomy; hypertension ;coagulopathy

研究者

发起方
Female Reproductive Research Center, Tabriz University of Medical Sciences

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