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Clinical Trial Summary

The purpose of this study is to evaluate the effectiveness and safety of a minimally invasive surgical procedure with ACT (Adjustable Continence Therapy) balloons implantation for the treatment of urinary incontinence in children with bladder exstrophy or isolated epispadias. The ACT therapy consists of two small adjustable silicone balloons connected with a tubing to a port, surgically placed around the bladder neck, one on each side of the urethra.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04935918
Study type Interventional
Source Assistance Publique Hopitaux De Marseille
Contact Alice FAURE, MD
Phone 04.91.96.81.41
Email alice.faure@ap-hm.fr
Status Recruiting
Phase N/A
Start date April 16, 2021
Completion date April 2028

See also
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