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OpenTrials
Completed

NCT Number: NCT04662398

Using of Testes' Shocker in Improving Sexual Activity

Using of testes' shocker in treating the sexual dysfunction.

Completed

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Key information

About this study

Using of electrical shocks in treating sexual dysfunction in males, rectile dysfunction and inability to perform sexually good.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • All patients with sexual dysfunction or erectile dysfunction

Exclusion criteria

  • Patients with trauma or other causes that make them inactive sexually

Treatment and study plan

JT Device

Device

Shocker giving electrical shocks on testes

Other names: Testes shocker

Primary outcomes

  1. Sexual desire

    Time frame: less than one month

    improving the desire of sex by using the electric shocks directly on the testes and penis. This will be assessed by a questionnaire (validated and reliable) to assess their ability to have sex more actively or not.

  2. Erectile dysfunction

    Time frame: less than one month

    solving the problem of erectile dysfunction and this will be assessed by examination and experience to see if there is an effect for the electric shocks on erectile improvement.

Sponsors and collaborators

Lead sponsor

University of Baghdad

Other

Registry information

Official study title

Using of Testes' Shocker in Treating Sexual Disease and Dysfunction

Important dates

Study start
2020
Primary completion
2021
Study completion
2021
First posted
Dec 10, 2020
Registry last updated
Nov 1, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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