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临床试验/IRCT201205309910N1
IRCT201205309910N1已完成2 期

Investigation of outcome of assessment reproduction treatment and prevention of ovarian hyper stimulation syndrome in GnRH agonist protocol compared to GnRH antagonist protocol

Isfahan University of Medical Sciences0 个研究点目标入组 136 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
入组人数
136

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 35 years(—)
性别
Female

入选标准

  • undergoing assisted reproduction techniques (ARTs) for the first time, age =35years and serum FSH level =10 IU/liter. Exclusion criteria: women with the previous history of IVF or ICSI; patients who had hyperprolactinemia, thyroid dysfunction, uterine abnormality, severe endometriosis and secondary infertility.

排除标准

  • 未提供

研究者

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