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Study identifier: NCT06822452 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Prospective Comparative Study Evaluating the Early Complications of Robot-assisted Radical Prostatectomy Performed as an Outpatient Versus an Inpatient Procedure.

Condition: Prostate Cancer Surgery · Ambulatory Care · Outpatient Surgery  ·  Sponsor: Elsan

PhaseNA
Planned participants510
Who can joinMale, 18 Years to no upper limit
Healthy volunteersNo

About this study

The goal of this clinical trial is to demonstrate that outpatient management for robotic-assisted radical prostatectomy is not inferior to inpatient management in terms of the occurrence of early post-operative complications. Researchers will compare outpatient robot-assisted radical prostatectomy to inpatient procedure. Participants will: * Visit the clinic after the operation once at 45 days, 6 months and once a year for up to 5 years for check-ups and tests. * Answer survey questions about urinary and erectil functions, stress and anxiety, satisfaction, quality of life for 6 months * Keep a diary to record procedures and treatments related to the care provided

This description comes directly from the study's public registry record.

Talk to the study team

Charlène PY, Eng  ·  +33556003048  ·  charlene.py@elsan.care

Always discuss trial participation with your own doctor first.

Locations (12)

Clinique Rhône DuranceAvignon, FranceNot Yet Recruiting
Clinique St VincentBesançon, FranceRecruiting
Clinique St AugustinBordeaux, FranceRecruiting
Polyclinique Médipôle St-RochCabestany, FranceRecruiting
Polyclinique du ParcCaen, FranceNot Yet Recruiting
Pole Sante Sud-CMCMLe Mans, FranceRecruiting
Hôpital Privé Nancy LorraineNancy, FranceNot Yet Recruiting
Polyclinique Les FleursOllioules, FranceRecruiting
Polyclinique Santé AtlantiqueSaint-Herblain, FranceNot Yet Recruiting
Clinique BelledonneSaint-Martin-d'Hères, FranceRecruiting
Centre clinicalSoyaux, FranceNot Yet Recruiting
Hôpital Privé OcéaneVannes, FranceRecruiting

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Source record: clinicaltrials.gov/study/NCT06822452