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Safety and Efficacy Study of USTRAP™ in Male Urinary Incontinence — PROSPECT  

Urinary Incontinence Clinical Trial

Official title:
Prospective Interventional Safety and Efficacy Study of USTRAP™ in Male Urinary Incontinence. An Open, Randomised, Multicentre Study Versus Artificial Sphincter.

Clinical Trial Summary

Few surgical methods to treat male stress urinary incontinence have been assessed in comparative, randomised interventional studies.

Ustrap is a new adjustable-pressure 4-arm device. The artificial sphincter is currently considered the gold standard device in this field.

The aim of this randomised prospective international study is to assess the efficacy and safety of the Ustrap® device comparatively with an artificial sphincter (AMS800) in the treatment of stress urinary incontinence following prostate removal in cancer patients.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03323554
Study type Interventional
Source Quanta Medical
Contact Jean Nicolas Cornu, MD,Professor
Phone 02 32 88 33 41
Email Jean-Nicolas.Cornu@chu-rouen.fr
Status Recruiting
Phase N/A
Start date June 1, 2018
Completion date November 1, 2027
View Details
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