Actively Recruiting
ESCAPE: Evaluation of Spinal Conservation by Endoscopic Procedures to Avoid Fusion
Led by University Hospital, Bordeaux · Updated on 2025-04-30
375
Participants Needed
13
Research Sites
54 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are investigating the use of endoscopic surgery as a less invasive alternative to traditional lumbar spine fusion for patients with spinal stenosis and spondylolisthesis. This approach aims to decompress the lumbar spine while preserving its natural function and stability, potentially reducing the need for spinal fusion. The study explores whether endoscopic techniques can lower the rate of more invasive surgical interventions in this population. The study focuses on patients who require spinal decompression surgery and are considered for endoscopic procedures. It observes outcomes related to these minimally destructive surgical methods without introducing experimental drugs or devices. The main goal is to evaluate the rate of surgical reintervention within one year after the initial endoscopic surgery. Participants will be monitored over time to assess if further surgical procedures are needed. Researchers will review medical imaging and clinical data to understand the effectiveness of endoscopic decompression in avoiding fusion surgery. The study involves adults 18 years and older and tracks outcomes related to surgical reintervention during the follow-up period, with participation potentially lasting up to several years.
CONDITIONS
Brief Title
ESCAPE : Evaluation of Spinal Conservation by Endoscopic Procedures to Avoid Fusion
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patient is 18 years old or older
- Patient consulting for a spinal pathology at the investigating center
- Presence of adjacent syndrome to a previous lumbar arthrodesis as defined by specific radiographic or MRI criteria
- Lumbar stenosis associated with lumbar scoliosis with vertebral rotation and Cobb angle greater than 20 degrees
- Indication for spinal surgery by endoscopy
You will not qualify if you...
- Patient under guardianship or curatorship
- Person deprived of liberty by judicial or administrative decision
- Person undergoing psychiatric treatment under duress requiring legal representative consent
- Person unable to express consent
- Person under legal protection
- Patient not affiliated with a social protection scheme
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 1 year
Participants who undergo routine care for spinal pathology are observed over time to evaluate surgical reintervention outcomes.
Periodic visits as part of routine clinical care
Trial Site Locations
Total: 13 locations
1
Hôpital Pellegrin, Centre Hospitalier Universitaire de Bordeaux
Bordeaux, France, 33000
Actively Recruiting
2
Clinique du dos de Bordeaux -Terrefort
Bruges, France, 33520
Actively Recruiting
3
CHU Lille
Lille, France, 59037
Not Yet Recruiting
4
Centre orthopédique SANTY
Lyon, France, 69008
Not Yet Recruiting
5
Centre orthopédique SANTY
Lyon, France, 69008
Not Yet Recruiting
6
Hôpital CLAIRVAL
Marseille, France, 13009
Actively Recruiting
7
CH de Narbonne
Narbonne, France, 11108
Actively Recruiting
8
Centre hospitalier Privé Sainte Marie
Osny, France, 95520
Not Yet Recruiting
9
Clinique du sport
Pessac, France, 33600
Actively Recruiting
10
Institut locomoteur de l'Ouest-Rachi
Saint-Grégoire, France, 35760
Actively Recruiting
11
Cabinet Orthosud Montpellier-Clinique Saint Jean
Saint-Jean-de-Védas, France, 34430
Actively Recruiting
12
Cabinet Orthosud Montpellier-Clinique Saint Jean
Saint-Jean-de-Védas, France, 34430
Actively Recruiting
13
Cabinet Orthosud Montpellier-Clinique Saint Jean
Saint-Jean-de-Védas, France, 34430
Actively Recruiting
Research Team
B
Benjamin BOUYER, PROF
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0