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Clinical Trial Summary

Shorten the time spent in the hospital (hospitalization duration) by optimizing the pre, per and postoperative care is of major medical and economic importance. Minimally invasive surgery allows a faster recovery than open surgery. However, we need to ensure an early and secure return to normality in order to discharge patients safely from the hospital. Clinical and biological parameters need to be controlled post-surgery. This work is going to evaluate the efficacity of a fast - recovery program with incoming patients receiving minimally invasive surgery (laparoscopic or robotic) of partial and total nephrectomy. The implementation of a medical and surgical fast-recovery program could - Lower the average duration of stay in hospital (at least by 1 day) with no increase of morbidity - Insure the absence of complications after 6 months home


Clinical Trial Description

Prospective study of a fast recovery program evaluating the impact on the hospitalization length and the incidence of re-hospitalization for complications for 60 patients undergoing a minimally invasive nephrectomy. The cohort will beneficiate of an extra preoperative information about the enhanced recovery after surgery program, they will benefit from a strategie of low morphine consumption during the per end post operative phase, they should need no bladder or abdominal drainage, they're encourage to eat and drink a few hours after surgery, the intravenous fluid is interrupted as early as possible, and the patients are encourage to sit, stand up and get dressed as soon as they are capable. A form completed by the patient registers their every day capabilities to eat, drink, move, and their limitations due to pain, dizziness, and nausea. Their bowel and urine transit are also registered. This form is complete until discharge from the hospital. Their laboratory test is monitored to identify kidney insufficiency or anemia and compared with the preoperative laboratory tests. The hospital discharge is allowed after medical and surgical criteria are met in both groups. A surgical evaluation is planned a week, one month, and 6 months after surgery with laboratory exams. 1 month after the discharge, a satisfaction questionnaire is filled up by the patient, answered by telephone. At the 6 months post operative consultation, a questionnaire about chronic pain is submitted. If the patient is eligible, a chronic pain consultation is further organized. The result will be compared to those of a retrospective cohort (+/- 60 patients) with no enhanced recovery after surgery program. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04601129
Study type Observational
Source University Hospital, Lille
Contact Gilles Lebuffe, MD,PhD
Phone 03 20 44 45 08
Email gilles.lebuffe@chru-lille.fr
Status Recruiting
Phase
Start date August 1, 2020
Completion date December 2023

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