跳至主要内容
临床试验/IRCT20211101052938N1
IRCT20211101052938N1已完成3 期

Comparison of the effect of oral progesterone and vaginal progesterone on luteal phase support using available drugs in IVF/ICSI candidates

Zanjan University of Medical Sciences0 个研究点目标入组 160 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
入组人数
160

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

  • IVF/ICSI candidate with history of infertility
  • age between 18 to 40 years old
  • have an informed consent to participate in the study

排除标准

  • drug reaction history to one of the drugs used in this study
  • endocrine or metabolic disorders
  • endometriosis
  • Azospermia of partner
  • uterine anatomic anomaly
  • history of 2 or more unsuccessful IVF or FET
  • history of repetitive spontaneous abortion

研究者

相似试验

Comparison of the effect of oral progesterone and... | 临床试验