U.S., March 13 -- ClinicalTrials.gov registry received information related to the study (NCT06873581) titled 'Pivotal Study of Voro Urologic Scaffold' on March 07.
Brief Summary: 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.
Study Start Date: March 31
Study Type: I...