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The effect of low-intensity shock waves (LI-ESWT) in patients with erectile dysfunction in comparison with medical treatment

Not Applicable
Recruiting
Conditions
Male erectile dysfunction.
Sexual arousal disorders
F52.2
Registration Number
IRCT20190824044601N1
Lead Sponsor
Mashhad University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Male
Target Recruitment
60
Inclusion Criteria

Men over 30 years old with at least 6 months elapsed since their erectile dysfunction and vasculogenic erectile dysfunction

Exclusion Criteria

Other erectile disorders include neurogenic, psychogenic and idiopathic disorders
History of pelvic surgery or radiotherapy
Use of anti-coagulants, use of anti-androgen
Anatomic penis deformities or prosthesis
Total testosterone lower than 8 nmol /dl,
Advanced heart or lung disease, neurological or psychiatric illness
Pregnant wife
International Index of Erectile Dysfunction More Than 25

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Increased at least 5 points on IIEF Erectile Dysfunction Questionnaire. Timepoint: The case group will be treated with ESWT weekly for 6 weeks. The control group will receive standard drug therapy (tadalafil) during this period. Patients in both groups will be evaluated at baseline, week 10 (4 weeks after treatment) and then every three months to one year. Method of measurement: International Index of Erectile Function Questionnaire.
Secondary Outcome Measures
NameTimeMethod
Score on Erection Hardness Score (EHS) questionnaire to over 3 in men with a lower or equal initial score. Timepoint: At baseline, 10 weeks (4 weeks after treatment) and then every three months to one year. Method of measurement: Erection Hardness Score questionnaire.
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