Condition: Radical Prostatectomy · Stress Urinary Incontinence (SUI) · Sponsor: Levee Medical, Inc.
The objective of this study is to compare safety and effectiveness of the Voro Urologic Scaffold in adult men undergoing robotic assisted radical prostatectomy as compared to control arm. The study is a multi-center, single blind, randomized, controlled trial. Up to 266 participants will be treated at up to 30 centers in the United States. The study will consist of a Baseline visit, implantation during robotic assisted radical prostatectomy (RARP), catheter removal, 6 weeks, 6 months, 12 months, 18 months, and 24 months.
This description comes directly from the study's public registry record.
Karen Cornett · 919-313-4520 · kcornett@leveemedical.com
Always discuss trial participation with your own doctor first.
| Mayo Clinic | Phoenix, Arizona, United States | Recruiting |
| Academic Urology | Sun City, Arizona, United States | Recruiting |
| University of California Los Angeles | Los Angeles, California, United States | Recruiting |
| University of California San Diego | San Diego, California, United States | Recruiting |
| Tampa General Hospital | Tampa, Florida, United States | Recruiting |
| University of Chicago Medicine | Chicago, Illinois, United States | Recruiting |
| IU school of Medicine, Department of Urology | Indianapolis, Indiana, United States | Recruiting |
| University of Maryland | Baltimore, Maryland, United States | Recruiting |
| John Hopkins | Baltimore, Maryland, United States | Recruiting |
| BMHCC/ Mississippi Urology Clinic | Jackson, Mississippi, United States | Recruiting |
| Northwell Health | New Hyde Park, New York, United States | Recruiting |
| Memorial Sloan Kettering Cancer Center | New York, New York, United States | Recruiting |
+ 7 more locations — full list on the registry record.
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Source record: clinicaltrials.gov/study/NCT06873581