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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05506722
Other study ID # TS2
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date September 1, 2022
Est. completion date January 1, 2023

Study information

Verified date October 2022
Source University of Baghdad
Contact Hashim Talib T Hashim, MBChB
Phone +964780257310
Email hashim.h.t.h@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Description:

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.


Recruitment information / eligibility

Status Recruiting
Enrollment 250
Est. completion date January 1, 2023
Est. primary completion date January 1, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria: - 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. Exclusion Criteria: - 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.

Study Design


Intervention

Device:
Testes shocker
It is a device that give electric shocks (up to 5 milli Amperes) and it is designed to contain both the testes within it.

Locations

Country Name City State
Iraq Al-Dar medical Center Nasiriyah Thi Qar

Sponsors (1)

Lead Sponsor Collaborator
University of Baghdad

Country where clinical trial is conducted

Iraq, 

Outcome

Type Measure Description Time frame Safety issue
Primary Semen analysis By taking the semen from the participants at baseline and then after each month and analyse it. 4 months
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