KCT0000157招募中未知
A multicentre, prospective randomized study to assess the effect when GnRH antagonist is started either on stimulation day 1 and day 6 vs. conventional GnRH agonist long protocol in patients with polycystic ovary syndrome undergoing IVF/ET
适应症
试验速览
- 阶段
- 未知
- 状态
- 招募中
- 入组人数
- 267
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional Study
入排标准
- 年龄范围
- 20(Year) 至 40(Year)（—）
- 性别
- Female
入选标准
- •PCOS patients (diagnosed as 2003 ASRM/ESHRE consensus meeting guideline)
- •age 20-40 years
- •patients who have normal uterus
排除标准
- •patients who have abnormal thyroid function
- •patients who have abnormal prolactin test
- •patients who have diabetes, or Cushing's syndrome, or congenital adrenal hyperplasia, or androgen-producing tumor.
- •Patients who reject informed consent
- •patients who have experience of adverse events for GnRH agonist, antagonist, recombinant FSH.
研究者
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