IRCT20101227005485N7已完成4 期
comparison of ovulation triggering outcome using these two methods: standard dose of human chorionic gonadotropin and human chorionic gonadotropin In combination with gonadotropin releasing hormone in IVF/ICSI cycles
适应症
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 入组人数
- 100
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
- 20 years 至 40 years（—）
- 性别
- Female
入选标准
- •women who are candidate of IVF/ICSI and have some risk of OHSS will be entered in the study.
排除标准
- •every body who have diminished ovarian reserve. (AFC<4 or AMH<1)
研究者
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