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临床试验/NCT01040247
NCT01040247终止不适用

Optimal Timing For Embryo Transfer For Low Responder Patients

HaEmek Medical Center, Israel1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2009年11月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
终止
入组人数
20
试验地点
1
主要终点
Pregnancy

研究概览

简要总结

Women undergoing in vitro fertilization (IVF) therapy, who are low responder and agree to enter the trial will be randomized to a study group, for whom embryo transfer will be done on the same day as oocyte aspiration and fertilization; and a control group for whom embryo transfer will be performed 48 to 72 hours later, as is the current accepted practice.

研究设计

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

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者
否

入选标准

  • •Patient undergoing IVF
  • •Number of mature oocytes equal to or lesser than the maximum number of embryos intended for transfer

排除标准

  • •Patient nor consenting

研究组 & 干预措施

Day 0 Embryo Transfer

Experimental

Embryo transfer will be performed on the same day as oocyte aspiration and fertilization

干预措施: Embryo Transfer (Other)

Day 2,3 Embryo Transfer

Active Comparator

Embryo Transfer will be performed 2 or 3 days after oocyte aspiration and fertilization

干预措施: Embryo Transfer (Other)

结局指标

主要结局

Pregnancy

时间窗: 14 days

次要结局

未报告次要终点

研究者

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

Amir Weiss

Senior Physician

HaEmek Medical Center, Israel

研究点 (1)

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