Using of Testes' Shocker in Improving Sexual Activity

October 31, 2022 updated by: Hashim Talib Hashim, University of Baghdad

Using of Testes' Shocker in Treating Sexual Disease and Dysfunction

Using of testes' shocker in treating the sexual dysfunction.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

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

Study Type

Interventional

Enrollment (Actual)

77

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Iraq
    • Thi Qar
      • Nasiriyah, Thi Qar, Iraq, 64001
        • Hashim Talib Talib Hashim

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Male

Description

Inclusion Criteria:

  • All patients with sexual dysfunction or erectile dysfunction

Exclusion Criteria:

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

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Triple

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Case (Testes shocker device)
The shocker will be used in delivering the current gradually on the testes and penis to improve the blood flow and stimulates the sexual activity among males.
Device: JT Device
Shocker giving electrical shocks on testes
Other Names:
  • Testes shocker
Sham Comparator: Control (non testes shocker device)
These groups will not given the shocks, shame device will be used instead and then compare the two results.
Device: JT Device
Shocker giving electrical shocks on testes
Other Names:
  • Testes shocker

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
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.
less than one month
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.
less than one month

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

University of Baghdad

Investigators

  • Principal Investigator: Ali Al Imam, MD, University of Mosul

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

December 5, 2020

Primary Completion (Actual)

January 14, 2021

Study Completion (Actual)

January 15, 2021

Study Registration Dates

First Submitted

November 28, 2020

First Submitted That Met QC Criteria

December 5, 2020

First Posted (Actual)

December 10, 2020

Study Record Updates

Last Update Posted (Actual)

November 1, 2022

Last Update Submitted That Met QC Criteria

October 31, 2022

Last Verified

October 1, 2022

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • HT98

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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