radical prostatectomy
ProcedureRobot-assisted
NCT Number: NCT06822452
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
Interested in participating?
Request Info18 year and older
Male
Interventional
Not applicable
Clinique Rhône Durance, Avignon, France
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Robot-assisted
Time frame: From the day of surgery to 8 days post-operative
The occurrence (yes/no) of at least one early complication of robot-assisted prostatectomy.
The early clinical complications expected are :
Time frame: Day of surgery
Patients treated on an outpatient basis for whom full hospitalisation is indicated on the day of surgery, as decided by the medical team.
Time frame: From enrollment to the day of surgery
Patients included in the study refusing outpatient care up to the day of surgery (before or after surgery) for whatever reason
Time frame: From hospital discharge to 8 days post-operative.
Patients readmitted to hospital (yes/no), emergency or inpatient department
Time frame: From hospitalisation discharge to 8 days post-operative
Early complication of robot-assisted prostatectomy
Time frame: From 8 days to 45 days post-operative
Patients who had at least one complication secondary to surgery.
The expected complications secondary to surgery are:
Time frame: From 45 days to 6 months post-operative
Patients who had at least one complication secondary to surgery.
Time frame: 3 days before surgery, day of surgery and 2 days post-operative
The participant's stress/anxiety level is assessed at 3 days before surgery using the APAIS (Amsterdam Preoperative Anxiety and Information Scale) questionnaire validated in French (Moerman and al, 1996; Maurice-Szamburski and al, 2013), then with a Numerical Scale of stress/anxiety during preparation for the operating theatre in the care unit and at 2 days post-operative.
Time frame: 2 days and 45 days post-operative
Patient satisfaction is assessed using the overall satisfaction question in the e-SATIS questionnaire ("Overall, how would you rate the quality of your treatment/care in the department by the doctors/surgeons/nurses? Bad/Weak/Average/Good/Excellent) The patient's opinion (yes/no) is evaluated on whether, if the procedure were repeated, the patient would accept it (yes/no) and whether it reassured him/her to go home in the evening /stay in hospital at night after the procedure.
Time frame: Day of surgery
Duration of surgery 'skin-to-skin' (incision until final stitch complete)
Time frame: Day of surgery
The level of blood loss is assessed by the quantity of blood recovered in the aspiration jar and the quantity from the drains minus the quantity perfused intraoperatively in ml.
Time frame: Baseline and 45 days post-operative
Urinary continence is assessed by the response to question 5 of the EPIC-50 (Expanded Prostate Cancer Index Composite) when 0 to 1 pads are used during the day by the patient. Recovery of urinary function was assessed by the difference between the incontinence subscore of the EPIC-50 questionnaire at D45 and the value of the pre-operative score.
The incontinence subscore include questions 1, 3, 4, 5 and 6a of the urinary function EPIC-50 questionnaire. The EPIC-50 is a validated questionnaire (Wei and al, 2000) and translated into French (Anota and al, 2016).
Time frame: Baseline and 45 days, 6 months after surgery
The evolution of continence and urinary function is established on the basis of the parameters defined previously (see Secondary Outcome Measure 12.)
Time frame: Baseline and 6 months post-operative
Erectile recovery is assessed using the IIEF-5 (International Index of Erectile Function) questionnaire (Rosen R and al, 1997; Dargis and al, 2013) ; erectile dysfunction is defined by an IIEF-5 score <10.
Time frame: From 45 days to 5 years after surgery
Recurrence is defined by a PSA (Prostate Specific Antigen) level >0.1ng/ml, the patient's re-treatment (yes/no), the type of re-treatment (hormone therapy / chemotherapy / radiotherapy).
Time frame: From hospital discharge to 6 months post-operative
The cost-utility ratio calculated on the basis of :
The following direct medical costs will be estimated from a societal perspective with a time horizon of 6 months:
Contact information is provided by the study sponsor or research team.
Elsan
Other
Acronym: PROSTAMBU
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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