Prospective Registry for female articifial urinary sphincter (VENUS)
Research type
Research Study
Full title
Prospective Registry for Patients Undergoing Artificial Urinary Sphincter Surgery for Female Stress Urinary Incontinence due to intrinsic sphincter deficiency
IRAS ID
283143
Contact name
Joni Kats
Contact email
Sponsor organisation
EAU Research Foundation
Duration of Study in the UK
5 years, 0 months, 1 days
Research summary
The aim of this study is to prospectively collect a pre-defined dataset from female patients who receive an artificial urinary sphincter (AUS) implantation for treatment of their stress urinary incontinence (SUI) from multiple centres in Europe. To provide insight in the daily clinical practice of the AUS implantation treatment and short- and long-term follow-up outcome (efficacy, complications, quality of life, urodynamic parameters, sexual function) of patients treated for SUI.
REC name
London - South East Research Ethics Committee
REC reference
20/LO/0901
Date of REC Opinion
9 Sep 2020
REC opinion
Further Information Favourable Opinion