Condition: Urinary Incontinence, Stress · Sponsor: Coloplast A/S
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.
This description comes directly from the study's public registry record.
Hugo Ryckebusch, Dr · +33 1 40 83 68 52 · frhr@coloplast.com
Martine Dehez · +33 9 83 54 12 45 · frmdeh@coloplast.com
Always discuss trial participation with your own doctor first.
| CHU Angers | Angers, France | Recruiting |
| Jean Minjoz Hospital | Besançon, France | Recruiting |
| CHU de Caen | Caen, France | Recruiting |
| Centre Hospitalier Chalon Sur Saône William Morey | Chalon-sur-Saône, France | Recruiting |
| Groupe Hospitalier Henri Mendor | Créteil, France | Terminated |
| Claude Huriez Hospital | Lille, France | Withdrawn |
| Clinique Mutualiste de la Porte de l'Orient | Lorient, France | Completed |
| Edouard Herriot Hospital | Lyon, France | Completed |
| Clinique de l'Esperance | Mougins, France | Completed |
| CHU Carémeau | Nîmes, France | Recruiting |
| Clinique Urologique Nantes-Atlantis | Saint-Herblain, France | Recruiting |
| Clinique Paul Picquet | Sens, France | Withdrawn |
+ 1 more locations — full list on the registry record.
Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.
We email about this public record only. Unsubscribe anytime with one click. Never medical advice.
This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.
Source record: clinicaltrials.gov/study/NCT04098822