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临床试验/IRCT201310311760N26
IRCT201310311760N26已完成3 期

Comparison of the efficiency of two short- term agonist protocols with conventional long protocol in women candidate Microinjection

Vice chancellor for research,Babol University of Medical Sciences0 个研究点目标入组 150 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
150

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
18 years 至 40 years(—)
性别
Female

入选标准

  • Inclusio criteria:
  • Healthy women 18 to 40 years; BMI = 20-32; Regular menstrual
  • Exclusion criteria:
  • Women PCOs; thyroid disorders, severe endometriosis, those with ovarian or uterine and ovarian pathology; FSH> 15 IU / LI on day 3 of the cycle; POOR RESPONSE; history of hyper stimulation in previous cycles; smokers; Abnormalities of the uterus, ovary-stimulating drugs or diet 2 months ago or the diet

排除标准

  • 未提供

研究者

发起方
Vice chancellor for research,Babol University of Medical Sciences

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