Evaluation of the effectiveness of Erectofix device for erectile dysfunctio

Phase 3

Recruiting

• Conditions: Erectile dysfunction.; Male erectile dysfunction, unspecified; N52.9

• Registration Number: IRCT20111121008146N40
• Lead Sponsor: Shahid Beheshti University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 29 August 2022

Recruitment & Eligibility

• Status: Recruiting
• Sex: Male
• Target Recruitment: 56

Inclusion Criteria

Age between 20-55 years
Has an erectile dysfunction problem

Exclusion Criteria

History of urological surgery with area nerve rupture, area vascular damage
History of orchiectomy
History of penile trauma with venous arterial fistula
History of trauma to the genital area that has caused neurological or vascular defects in the area.
History of taking antipsychotic drugs and benzodiazepines, anti-androgens
History of medical conditions (diabetes, hypertension, hyperlipidemia, thyroid disorders and major depression)
History of smoking, alcohol and drugs, as well as a history of occupational exposure to chemicals and radioactive substances.

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Erectile dysfunction. Timepoint: Before intervention and one week after the last intervention. Method of measurement: Male sexual function refers to the score that a person obtains in the International Male Erectile Performance Index Questionnaire (Rosen et al., 1997).