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临床试验/NCT02335736
NCT02335736Unknown2 期

Can Antagonist Protocol be the Protocol of Choice in in Vitro Fertilization Patients?

Woman's Health University Hospital, Egypt1 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2015年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
发起方
入组人数
200
试验地点
1
主要终点
number of oocytes collected and fertilized

研究概览

简要总结

The antagonist protocol in a novel method of stimulation in the in vitro fertilization (IVF) patients. It has been tried in poor responders, polycystic ovary (PCO) patients and normal females undergoing IVF. Can it be used with the same efficacy in all patients?

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
20 Years 至 44 Years(Adult)
性别
Female
接受健康志愿者
是

入选标准

  • •age: 20- 44 years
  • •Poor responder females according to Bologna criteria
  • •Polycystic ovarian disease females according to Rotterdam criteria
  • •Females with infertility causes other than poor responders, or PCO; male factor or tubal block

排除标准

  • •refusal to get enrolled in the study
  • •cases of infertility due to severe male factor

研究组 & 干预措施

Normal

Active Comparator

Human menopausal gonadotrophin IM daily was administrated from day 2 of the cycle. The Gonadotropins releasing hormone antagonist GnRH ant (Cetrotide, Serono, Geneva, Switzerland) was given when the leading follicle was from 12 to 14 mm, at a daily dose of 0.25 mg SC.

干预措施: Gonadotropins releasing hormone antagonist (Drug)

Poor responders

Active Comparator

Human menopausal gonadotrophin IM daily was administrated from day 2 of the cycle. The Gonadotropins releasing hormone antagonist GnRH ant (Cetrotide, Serono, Geneva, Switzerland) was given when the leading follicle was from 12 to 14 mm, at a daily dose of 0.25 mg SC

干预措施: Gonadotropins releasing hormone antagonist (Drug)

Polycystic ovarian disease

Active Comparator

Human menopausal gonadotrophin IM daily was administrated from day 2 of the cycle. The Gonadotropins releasing hormone antagonist GnRH ant(Cetrotide, Serono, Geneva, Switzerland) was given when the leading follicle was from 12 to 14 mm, at a daily dose of 0.25 mg SC

干预措施: Gonadotropins releasing hormone antagonist (Drug)

结局指标

主要结局

number of oocytes collected and fertilized

时间窗: 6 months

次要结局

未报告次要终点

研究者

发起方
Woman's Health University Hospital, Egypt
申办方类型
Other
责任方
Principal Investigator
主要研究者

Dina Mohamed Refaat Dakhly

lecturer of obstetrics and gynecology

Woman's Health University Hospital, Egypt

研究点 (1)

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