Actively Recruiting

Age: 18Years +
All Genders
ID06950853

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Long-term Monitoring

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

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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

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