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Clinical Trials/NCT04662398
NCT04662398CompletedNot Applicable

Using of Testes' Shocker in Treating Sexual Disease and Dysfunction

University of Baghdad1 site in 1 country77 target enrollmentStarted: December 5, 2020Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
77
Locations
1
Primary Endpoint
Sexual desire

Study Overview

Brief Summary

Using of testes' shocker in treating the sexual dysfunction.

Detailed Description

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

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Triple (Participant, Care Provider, Outcomes Assessor)

Eligibility Criteria

Ages
20 Years to — (Adult, Older Adult)
Sex
Male
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •All patients with sexual dysfunction or erectile dysfunction

Exclusion Criteria

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

Arms & Interventions

Case (Testes shocker device)

Active Comparator

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.

Intervention: JT Device (Device)

Control (non testes shocker device)

Sham Comparator

These groups will not given the shocks, shame device will be used instead and then compare the two results.

Intervention: JT Device (Device)

Outcomes

Primary Outcomes

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.

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.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Hashim Talib Hashim

Medical Student

University of Baghdad

Study Sites (1)

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