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Shock-wave therapy in men with pelvic pai

Phase 3
Conditions
Chronic Pelvic Pain Syndrome (Chronic Prostatitis).
Chronic prostatitis
Registration Number
IRCT2017082635911N1
Lead Sponsor
Vice chancellor for research, Shahid Beheshti University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Male
Target Recruitment
34
Inclusion Criteria

>18 years old; definite diagnosis of CPPS; Symptomatic for at least 3 months; no treatment before; sign the informed consent
Exclusion criteria:
acute or chronic bacterial prostatitis; UTI in 1 recent year; history of prostate cancer or PSA>4; coagulation problems; history of hematuria, urethral stricture, urologic cancers, urolithiasis, neurogenic bladder, STDs, colorectal problems, inguinal hernia and varicocele; drug addiction

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain. Timepoint: before, 1 and 3 months after procedure. Method of measurement: Visual Analog Scale Questionnaire.;Qmax. Timepoint: before, 1 and 3 months after procedure. Method of measurement: Uroflowmetry.;Erectile Dysfunction. Timepoint: before, 1 and 3 months after procedure. Method of measurement: International Index of Erectile Function 5 Questionnaire.;Symptoms Severity. Timepoint: before, 1 and 3 months after procedure. Method of measurement: National Institute of Health Chronic Prostatitis Index Questionnaire.;Lower urinary Tract Symptoms. Timepoint: before, 1 and 3 months after procedure. Method of measurement: International Prostate Symptom Score Questionnaire.
Secondary Outcome Measures
NameTimeMethod
Hematuria. Timepoint: 1 and 3 months after procedure. Method of measurement: Inreview.;Hematospermia. Timepoint: 1 and 3 months after procedure. Method of measurement: Interview.;Post void residue. Timepoint: before, 1 and 3 months after. Method of measurement: uroflowmetry.
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