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Study identifier: NCT05874375 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

UCon Treatment of Overactive Bladder (OAB) in Males

Condition: Urinary Incontinence · Urge Incontinence · Nocturia  ·  Sponsor: InnoCon Medical

PhaseNA
Planned participants20
Who can joinMale, 18 Years to no upper limit
Healthy volunteersNo

About this study

UCon is a medical device for treatment of the symptoms of OAB and fecal incontinence (FI). It electrically stimulates the DGN through the skin to obtain modulated behaviour of the bladder musculature e.g., suppress undesired bladder activity to relieve the symptoms of the patient. This clinical investigation is a randomized, cross-over, single-site, prospective, early feasibility study, which is used to evaluate Ucon with respect to its initial clinical safety and device performance in a small number of males with OAB.

This description comes directly from the study's public registry record.

Talk to the study team

Dianna Mærsk Knudsen  ·  40517712  ·  dmk@innoconmedical.dk

Always discuss trial participation with your own doctor first.

Locations (1)

Maastricht University Medical Center+Maastricht, NetherlandsRecruiting

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Source record: clinicaltrials.gov/study/NCT05874375