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Clinical Trials in France / NCT06950853
Recruiting Observational

ESCAPE : Evaluation of Spinal Conservation by Endoscopic Procedures to Avoid Fusion

NCT06950853 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2024-02-01
Last updated
2025-04-30

Condition(s) studied

Spinal StenosisSpondylolisthesis

Study summary

The recent development and expansion of endoscopic surgery has made it possible to offer an alternative to this therapeutic escalation. This method allows decompression procedures to be performed using optimized and minimally destructive surgical approaches, which contributes to preserving the physiological function of the lumbar spine and in particular its stability.

The main hypothesis of the research is that the use of endoscopic techniques for decompression of the lumbar spine allows a reduction in the indication for lumbar arthrodesis.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patient ≥ 18 years old * Patient consulting for a medical reason involving a spinal pathology in the investigating center : Syndrome adjacent to an old lumbar arthrodesis defined on preoperative radiographs by an antero-posterior translation \> 3 mm, segmental kyphosis \> 10° or a disc height reduced by more than 50%, or on preoperative MRI by central stenosis of grade C or D of the Schizas classification or a herniated disc Grade 1 or 2 degenerative spondylolisthesis, i.e. with slippage less than 50% of the depth of the underlying vertebral body. Lumbar stenosis complicating lumbar scoliosis defined by a deformation with rotation of the vertebral bodies on a frontal radiograph (absence of centering of the spinous process between the two pedicles of the vertebra concerned) and a Cobb angle greater than 20° or a rotational dislocation . \- Indication for spinal surgery by endoscopy Exclusion Criteria: * Patient under guardianship or curatorship, * Persons deprived of liberty by judicial or administrative decision, * Persons undergoing psychiatric treatment under duress requiring the consent of the legal representative * Persons unable to express their consent, * Persons under legal protection, * Patient not affiliated to a social protection scheme.

Primary outcome measure(s)

Trial sites (13)

FacilityCityRegionStatus
Hôpital Pellegrin, Centre Hospitalier Universitaire de Bordeaux Bordeaux France Recruiting
Clinique du dos de Bordeaux -Terrefort Bruges France Recruiting
CHU Lille Lille France Not Yet Recruiting
Centre orthopédique SANTY Lyon France Not Yet Recruiting
Centre orthopédique SANTY Lyon France Not Yet Recruiting
Hôpital CLAIRVAL Marseille France Recruiting
CH de Narbonne Narbonne France Recruiting
Centre hospitalier Privé Sainte Marie Osny France Not Yet Recruiting
Clinique du sport Pessac France Recruiting
Institut locomoteur de l'Ouest-Rachi Saint-Grégoire France Recruiting
Cabinet Orthosud Montpellier-Clinique Saint Jean Saint-Jean-de-Védas France Recruiting
Cabinet Orthosud Montpellier-Clinique Saint Jean Saint-Jean-de-Védas France Recruiting
Cabinet Orthosud Montpellier-Clinique Saint Jean Saint-Jean-de-Védas France Recruiting

More University Hospital, Bordeaux trials in France

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06950853 on ClinicalTrials.gov ↗ ← All trials in France