Spine Surgery Clinical Trial
Official title:
Evaluation of an Enhanced Recovery Protocol After Minimally Invasive Lumbar Surgery.
Prospective longitudinal multicentre observational study carried out on a population of patients undergoing minimally invasive spine surgery and divided into two parallel cohorts according to the presence or absence of a Enhanced Recovery After Surgery (ERAS) programme. The patient will be assessed during 4 visits: At inclusion before surgery, at D0 (day of surgery), at D1 (postoperative visit) and at M1 (follow-up visit).
On a population of patients undergoing minimally invasive lumbar spine surgery divided into two cohorts of equal size according to the presence or absence of a Enhanced Recovery After Surgery (ERAS) programme: Primary objective To compare the percentage of therapeutic success achieved in each group one month after surgery. Secondary objectives: to compare between groups: - Postoperative pain intensity at D1 and M1 - Analgesic consumption (in stages) at D1 and M1 - Pain-free walking distance at M1 - Surgery conditions (duration of operation, duration of hospitalisation) - Frequency of adverse events related to surgery (infection rate, 1 month recovery rate, transfusion requirements) - Emotional impact of the management ;
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