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临床试验/NCT05506722
NCT05506722招募中不适用

The Using of the Testes' Shocker in Improving the Sperms' Activity and the Spermatogenesis Process Among Infertile Men

University of Baghdad1 个研究点 分布在 1 个国家目标入组 250 人开始时间: 2022年9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
招募中
入组人数
250
试验地点
1
主要终点
Semen analysis

研究概览

简要总结

Infertility was reported in approximately 15% of all heterozygous couples, with male factor accounting for nearly half the cases. This typically occurs due to low sperm production, sperm dysfunction, and sperm delivery obstruction. Etiology of male infertility can be attributed to many factors including acute or chronic illness, accidents, and lifestyle choices.

详细描述

This study demonstrated that using a painless, convenient at-home device could significantly improve sperm motility and count. This device can be utilized to tackle (for unexplained infertility) the significant issue of infertility in a cost-effective, safe and efficacious.

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

盲法说明

By mixing the devices together and giving them to the participants blindly.

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
Male
接受健康志愿者
是

入选标准

  • •Infertile male with oligosperma, necrospermia, asthenozoospermia or hypospermia. Must not taking any drugs or medications for infertility and has nit any congenital diseases in the genital tracts or chronic diseases.

排除标准

  • •Have congenial genital tract disease, has a chrome disease, has other than the above mentioned causes for infertility or taking medications that can affect the fertility.

研究组 & 干预措施

Testes shocker

Active Comparator

This device is working and giving the electrical shocks regularly.

干预措施: Testes shocker (Device)

Fake Testes shocker

Placebo Comparator

This device is not giving electricity but it is working with a red light, so the participants cannot suspect it.

干预措施: Testes shocker (Device)

结局指标

主要结局

Semen analysis

时间窗: 4 months

By taking the semen from the participants at baseline and then after each month and analyse it.

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

Hashim Talib Hashim

Doctor (MBChB)

University of Baghdad

研究点 (1)

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