BridgeMD
Compares treatment options for Prostate Cancer Surgery
Official title Prospective Comparative Study Evaluating the Early Complications of Robot-assisted Radical Prostatectomy Performed as an Outpatient Versus an Inpatient Procedure.
ClinicalTrials.gov ID: NCT06822452
What this study is testing
- What it's testing
- 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.
- Time commitment: about 5 years
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 and older, men only
You may be able to join if
- Male, aged 18 and over
- Patient with prostate cancer for which the multidisciplinary meeting has proposed radical prostatectomy as a therapeutic option (with or without...
- Patient eligible for outpatient treatment :
- The patient undertakes to comply with all medical instructions given during surgical consultations and the anaesthetic consultation.
- The patient has access to personal transport allowing, if necessary, return to the facility or another approved facility (transport time and distance...
You likely can't join if
- Patient already treated for prostatic carcinoma with brachytherapy, radiotherapy or focal therapy
- Patient participating in ongoing research or in a period of exclusion at the time of inclusion
- Refusal or inability to comply with the study protocol for any reason whatsoever
- Protected participant: adult under guardianship, curatorship or other legal protection, deprived of liberty by judicial or administrative decision.
See the full eligibility criteria
- Male, aged 18 and over
- Patient with prostate cancer for which the multidisciplinary meeting has proposed radical prostatectomy as a therapeutic option (with or without lymphadenectomy)
- Patient eligible for outpatient treatment :
- The patient undertakes to comply with all medical instructions given during surgical consultations and the anaesthetic consultation.
- The patient has access to personal transport allowing, if necessary, return to the facility or another approved facility (transport time and distance from the facility are not exclusion factors)
- The patient has access to telephone communication facilities.
- The patient undertakes not to drive a vehicle and to be accompanied on his return home and for the next 24 hours by a responsible person who will be familiar with the monitoring instructions.
- The patient plans to remain in hospital overnight if this is deemed necessary by the department's doctors (operator and anaesthetist). The patient accepts this mode of care and its constraints.
- Participant affiliated to or benefiting from a social security scheme
- The participant has been informed and has given his/her free, informed and written consent (at the latest on the day of inclusion and before any examination required by the research).
- Patient already treated for prostatic carcinoma with brachytherapy, radiotherapy or focal therapy
- Patient participating in ongoing research or in a period of exclusion at the time of inclusion
- Refusal or inability to comply with the study protocol for any reason whatsoever
- Protected participant: adult under guardianship, curatorship or other legal protection, deprived of liberty by judicial or administrative decision.
The study team makes the final eligibility decision.
Where it's taking place
- Avignon, France
- Besançon, France
- Bordeaux, France
- Cabestany, France
- Caen, France
- Le Mans, France
- Nancy, France
- Ollioules, France
- Saint-Herblain, France
- Saint-Martin-d'Hères, France
- Soyaux, France
- Vannes, France
Compensation & support
Compensation mentioned.
ClinicalTrials.gov doesn't provide a reliable structured field for payment or travel support - confirm details with the study team.
Questions & answers
Do participants get paid in this trial?
This study's listing includes signals that participants may be compensated or receive a stipend. Amounts vary and are set by the study team - confirm the details with them.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The study runs about 5 years per participant, based on its public description. The team confirms the exact schedule and number of visits before you enroll.
Who can join this trial?
This study is enrolling male, 18 years and older. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Avignon, France; Besançon, France; Bordeaux, France; Cabestany, France; Caen, France; Le Mans, France and 6 more location(s). Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.