CTRI/2017/11/010317进行中（未招募）3 期
A randomized, open label, assessor-blind, parallel group, multi centre Phase III study to compare the efficacy and safety of r-hMG and HP-hMG in subjects undergoing controlled ovarian stimulation for ART
Bharat serums and Vaccines ltd0 个研究点目标入组 309 人开始时间: 待定最近更新:
试验速览
- 阶段
- 3 期
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 309
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
入选标准
- •Subject has an indication for ART using COS.
- •regular menstural cycle.
- •FSH level less
- •Estradiol level less,
- •AFC of 10- 25
- •BMI more than 18.5 and less than 30 kg/m2
排除标准
- •1 history of >2 successive ART cycles without clinical pregnancy
- •2. history of any endocrine abnormality
- •3. history of OHSS
- •4. documented PCOS
- •5. having Ovarian abnormality
- •6. documented severe endometriosis
- •7. having submucosal fibroid
- •8. history of extrauterine pregnancy in past 3 months
- •9. History of miscarriages
- •10. Poor response to gonadotropin treatment
- •11. Positive HIV, Hepatits B, C
- •12. Known case of allergic, hypersensitive, to r-hmg, or its excipients.
- •13. history of other co morbid condition that prevent in participating in trial under investigators discretion.
- •14. history of addiction
研究者
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