A 3 Years Naturalistic Cohort Survey Of Virtue® Male Sling System For Male Stress Urinary Incontinence A Post-marketing and Multicenter Prospective Observational Cohort in Subjects With Male Stress Urinary Incontinence
Status: Recruiting
Location: See all (13) locations...
Intervention Type: Device
Study Type: Observational
SUMMARY
The purpose of this study is to monitor the use of Virtue® Male Sling in a real world population and collect medical data on effectiveness and to monitor safety of Virtue® at 12 and 36 months post device implantation in men with post-prostatectomy urinary incontinence.
Eligibility
Participation Requirements
Sex: Male
Minimum Age: 18
Healthy Volunteers: f
View:
• Implanted with the Virtue® Male Sling System
Locations
Other Locations
France
CHU Angers
RECRUITING
Angers
Jean Minjoz Hospital
RECRUITING
Besançon
CHU de Caen
RECRUITING
Caen
Centre Hospitalier Chalon Sur Saône William Morey
RECRUITING
Chalon-sur-saône
Groupe Hospitalier Henri Mendor
TERMINATED
Créteil
Claude Huriez Hospital
WITHDRAWN
Lille
Clinique Mutualiste de la Porte de l'Orient
COMPLETED
Lorient
Edouard Herriot Hospital
COMPLETED
Lyon
Clinique de l'Esperance
COMPLETED
Mougins
CHU Carémeau
RECRUITING
Nîmes
Clinique Urologique Nantes-Atlantis
RECRUITING
Saint-herblain
Clinique Paul Picquet
WITHDRAWN
Sens
Italy
Ospedale Generale Regionale F. Miull
WITHDRAWN
Acquaviva Delle Fonti
Contact Information
Primary
Hugo Ryckebusch, Dr
frhr@coloplast.com
+33 1 40 83 68 52
Backup
Martine Dehez
frmdeh@coloplast.com
+33 9 83 54 12 45
Time Frame
Start Date: 2017-06-29
Estimated Completion Date: 2026-12
Participants
Target number of participants: 130
Authors
Bertrand Rabut, René Yiou, Giuseppe Ludovico
Related Therapeutic Areas
Sponsors
Leads: Coloplast A/S