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Clinical Trial Summary

This research study is trying to determine if Low-Intensity shock wave therapy (LiSWT) is safe and effective in patients with symptoms of erectile dysfunction (ED) after radical prostatectomy.


Clinical Trial Description

Participants will be randomized to the active treatment group or the control/placebo group. All patients on active treatment will receive Low-Intensity shock wave treatment. Participants assigned to the control group will receive the treatment using a sham applicator. The placebo group will receive the same treatment as the active group, but the transducer used for shock wave treatment will be capped, meaning that no shock waves will be transmitted to the penis. Participants on active shock wave treatment will receive once a week Low-Intensity shock wave treatments of 0.2 mJ/ mm² over the lateral penile shaft (distal, mid, and proximal penile shaft), 500 impulses in each area, for a total of 1500 shocks along the penis once a week for six weeks, with a total of 6 treatments once a week. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06219785
Study type Interventional
Source The Methodist Hospital Research Institute
Contact Manuel Villarreal
Phone 3462386122
Email mvillarreal2@houstonmethodist.org
Status Recruiting
Phase N/A
Start date January 10, 2024
Completion date June 30, 2026

See also
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