临床试验/CTRI/2024/05/067437

CTRI/2024/05/067437尚未招募不适用

Use of soluble human leukocyte antigen (sHLA-G) as potential biomarker of embryo quality for clinical outcomes in women undergoing IVF/ICSI non-donor cycles â€“ A Prospective Observational Study

All India Institute of Medical Science1 个研究点分布在 1 个国家目标入组 100 人开始时间: 2024年6月14日最近更新: 2024年5月9日

适应症

试验速览

阶段: 不适用
状态: 尚未招募
发起方: All India Institute of Medical Science
入组人数: 100
试验地点: 1
主要终点: Assessing influence of sHLA-G on Day-3 embryo quality

研究概览研究设计入排标准结局指标研究者研究点记录与标识符相似试验

研究概览

简要总结

In this study soluble human leukocyte antigen will be assessed from day 3 spent culture media. depend on its value embryo quality will be assessed and embryo transfer will be performed accordingly. in this study we want assess whether soluble human leukocyte antigen is a potential maker for embryo quality. Study is not yet started.

研究设计

研究类型: Observational

入排标准

年龄范围: 21.00 Year(s) 至 38.00 Year(s)（—）
性别: Female

入选标准

•normo/hyper-responders, tubal factor, endometriosis, mild male factor infertility.

排除标准

•oncofertility patients, donor recipient cycles, diminished ovarian reserve, male factor infertility,.

结局指标

主要结局

Assessing influence of sHLA-G on Day-3 embryo quality

时间窗: Day 3 Embryo quality

次要结局

Evaluating the quantitative analysis of sHLA-G in relation to the quality of embryos on Day 3, evaluating the quantitative analysis of sHLA-G in relation to the quality of embryos on Day 5, Evaluating the influence of sHLA-G on implantation rate, clinical pregnancy rate & on ongoing pregnancy rate(Day 3 embryo quality, day 5 embryo quality, after 2weeks of embryo transfer, at 6weeks of pregnancy)

研究者

发起方

All India Institute of Medical Science

申办方类型

Research institution and hospital

责任方

Principal Investigator

主要研究者

Dr. Nisha

AIIMS,NEW DELHI

研究点 (1)

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