跳至主要内容
临床试验/PACTR201911748191910
PACTR201911748191910尚未招募未知

Optimal Time Interval Between Final Follicular Triggering by Human Chorionic Gonadotropin and Ovum Pickup and Outcome of Gonadotropin Releasing Hormone Antagonist ICSI Cycles

Department of obstetrics and Gynecology Faculty of medicine Alexandria University0 个研究点目标入组 400 人开始时间: 2019年11月2日最近更新:
适应症

试验速览

阶段
未知
状态
尚未招募
发起方
入组人数
400

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
19 Year(s) 至 44 Year(s)(—)
性别
Female

入选标准

  • Women aged 20 – 35 years
  • with expected normal response to the standard controlled ovarian stimulation
  • undergo ICSI for any cause of infertility.

排除标准

  • 1.Cases of polycystic ovaries syndrome (PCOS).
  • 2.Women with history of ovarian hyper-response and/or OHSS in previous ICSI cycle.
  • 3.Women with history of poor ovarian response according to Bologna criteria.
  • 4.Antimullerian hormone level either < 1.1 ng/dl or > 4.0 ng/dl.
  • 5.Surgically retrieved sperms.
  • 6.Untreated hydrosalpinges.
  • 7.Congenital uterine abnormalities.

研究者

发起方
Department of obstetrics and Gynecology Faculty of medicine Alexandria University

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