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临床试验/NCT03533803
NCT03533803已完成3 期

Indomethacin Prior to Difficult Embryo Transfer is it a Solution?

Cairo University1 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2018年6月2日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
200
试验地点
1
主要终点
Implantation rate

研究概览

简要总结

IVF/ICSI patients who had difficult mock embryo transfer on the day of ovum pick up. Will be randomly assigned into two groups; group A will receive 100mg indomethacin rectal suppository 1-2 hours before ET and group B will not receive indomethacin

研究设计

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

入排标准

年龄范围
20 Years 至 38 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Infertile patients undergoing IVF cycle with difficult mock embryo transfer
  • Early follicular FSH level ≤10 IU/L.
  • Tubal, male infertility and unexplained causes of fertility will be recruited.
  • Fresh ET.

排除标准

  • Repeated IVF failure.
  • Past history of allergy to NSAID, bronchial asthma , peptic ulcer or inflammatory bowel disease.
  • Easy mock embryo transfer.

研究组 & 干预措施

Group A (Indomethacin)

Active Comparator

All patient had long stimulation protocol and IVF/ICSI. After mock embryo transfer women with any degree of difficulty will receive Indomethacin 100Mg Suppository 1-2 hours before embryo transfer.

干预措施: Indomethacin 100Mg Suppository (Drug)

Group A (Indomethacin)

Active Comparator

All patient had long stimulation protocol and IVF/ICSI. After mock embryo transfer women with any degree of difficulty will receive Indomethacin 100Mg Suppository 1-2 hours before embryo transfer.

干预措施: IVF/ICSI (Procedure)

Group B (Control)

Placebo Comparator

All patient had long stimulation protocol and IVF/ICSI. After mock embryo transfer women with any degree of difficulty will not receive any medications before embryo transfer.

干预措施: IVF/ICSI (Procedure)

结局指标

主要结局

Implantation rate

时间窗: 6 weeks

the number of total gestational sacs divided by the total number of embryos transferred.

次要结局

  • Ongoing pregnancy rate(12 weeks)
  • Clinical pregnancy rate(6 weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Yasmin Ahmed Bassiouny

Assistant Professor of Obstetrics and Gynaecology

Cairo University

研究点 (1)

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