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临床试验/NCT04675164
NCT04675164已完成不适用

Outcome of ICSI Using Laser Assisted Sperm Selection of Viable Immotile Testicular Sperm in Azoospermic Infertile Men: a Randomized Controlled Trial

Sohag University1 个研究点 分布在 1 个国家目标入组 168 人开始时间: 2020年10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
已完成
入组人数
168
试验地点
1
主要终点
Clinical pregnancy rate

研究概览

简要总结

This study aims to investigate the outcome of ICSI after using LAISS for selection of viable immotile testicular sperm in azoospermic infertile men.

Patients will be randomly assigned to 2 groups. In (LAISS) group, viable immotile testicular sperms will be selected before ICSI using laser assisted immotile sperm selection (study group). In (HOST) group, viable immotile testicular sperms will be selected before ICSI using hypo-osmotic swelling test (control group).

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
Triple (Participant, Care Provider, Outcomes Assessor)

盲法说明

With an online tool, participants will be randomized to undergo ICSI with HOST and LAISS sperm selection arms with a 1:1 allocation ratio as per a computer-generated list, using permuted block sizes of 8, and 16, stratified for sites and fresh or cryopreserved sperm. Results of allocation will be in sealed opaque envelopes labeled with unique random codes. Clinicians, embryologists, and participants in all centers will have no access to allocation results. Upon consent, instructors will assign participants to the relevant group. Embryologists who will perform fertilization check and embryo grading will be unaware of the sperm selection method. Women will undergo only day 5 blastocysts transfer. This trial will also conceal the allocation from participants and clinical team.

入排标准

年龄范围
18 Years 至 35 Years(Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Eligible couples are those undergoing ICSI due to azoospermia with testicular biopsy positive for sperm (either fresh or cryopreserved) following testicular sperm extraction (TESE) or aspiration (TESA).

排除标准

  • •Cases with female factor infertility or woman age above 35 years will be excluded.

研究组 & 干预措施

LAISS group

Active Comparator

Viable immotile testicular sperms will be selected before ICSI using laser assisted immotile sperm selection (study group).

干预措施: Laser Assisted Immotile Sperm Selection (Device)

HOST group

Active Comparator

Viable immotile testicular sperms will be selected before ICSI using hypo-osmotic swelling test (control group).

干预措施: Hypo-osmotic Swelling Test (Procedure)

结局指标

主要结局

Clinical pregnancy rate

时间窗: 6- 7 weeks

Presence of a fetal heartbeat at 6-7 weeks of pregnancy.

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

Mohamed Alaa El-Dein Hasan

Assistant Lecturer of Dermatology, Venreology and Andrology

Sohag University

研究点 (1)

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