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Clinical Trial Summary

The purpose of the study is to evaluate the incidence of surgery-related complications between Day 0 and Day 30.


Clinical Trial Description

This is an observational, prospective, open, non-comparative (single arm), bicentric study. This study is aimed at patients with prostate cancer for whom an ambulatory laparoscopic radical prostatectomy has been validated at a multidisciplinary consultation meeting. The possibility of performing this procedure on an outpatient basis is left to the surgeon's discretion, according to well-defined medical procedure criteria. This cohort is part of the usual care. The study will observe the incidence and describe the type, number, severity, duration and frequency of procedure-related complications that may arise in the first month post-op of ambulatory Laparoscopic Radical Prostatectomy. For this reason, patient follow-up will stop at 1 month after surgery, during a routine follow-up visit. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05975775
Study type Observational
Source GCS Ramsay Santé pour l'Enseignement et la Recherche
Contact Arnaud BALDINI, MD
Phone 469001019
Email docteur.baldini@urolyon-ouest.fr
Status Recruiting
Phase
Start date October 20, 2023
Completion date December 2024

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