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Clinical Trial Summary

The study will include 50 chronic pelvic pain syndrome (CPPS) patients who will be randomised in 2 groups. Group A (25 patients )will receive 6 LiST sessions with a frequency 1 session / week. Group B (25 patients) will receive 6 LiST sessions with a frequency 2 sessions / week. National Institutes of Health Chronic Prostatitis Symptom Index(NHI-CPSI), International Prostate Symptom Score (IPSS), International Index of Erectile Function (IIEF-ED) questionnaires will be answered before and at 1 and 3 month follow up visit. Adverse events will be reported during the treatment and follow up period.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04549389
Study type Interventional
Source Institute for the Study of Urological Diseases, Greece
Contact
Status Completed
Phase N/A
Start date March 2, 2020
Completion date January 15, 2021

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