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Clinical Trial Summary

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.


Clinical Trial Description

The purpose of the current investigation is to obtain information about the type of stimulation that Ucon provide (time limited vs. urge stimulation), would be the most effective and feasible for the treatment of non-neurogenic OAB symptoms in males. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05874375
Study type Interventional
Source InnoCon Medical
Contact Dianna Mærsk Knudsen
Phone 40517712
Email dmk@innoconmedical.dk
Status Recruiting
Phase N/A
Start date October 12, 2023
Completion date October 12, 2024

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