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Selection of Chronic Low Back Pain Patients for Neurotomy Surgery Radiofrequency

Unknown statusNCT05624307
View the official record on ClinicalTrials.gov

Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.

This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.

Brief summary (from the registry)

Chronic low back pain is one of the leading causes of disability associated with significant health care costs. One possible management of chronic low back pain of facet origin is neurotomy-radiofrequency (NT-RF) intervention. Currently, to determine whether a patient is eligible for NT-RF, two positive block tests are required. Clinical examination with a homolateral extension-rotation-tilt maneuver of the spine (ERI maneuver) would have the potential to identify subjects with pain of facet origin. It could therefore be a simple and effective diagnostic tool in the evaluation of a patient with low back pain and help in the decision whether or not to perform a test block by local infiltration of the zygapophyseal joint prior to an NT-RF procedure. The purpose of this longitudinal, prospective, observational, single-center study is to evaluate the performance of the combined extension-rotation-lateral tilt maneuver (ERI maneuver) in predicting the response to neurotomy-radiofrequency intervention in patients with chronic low back pain. The included patients will answer 5 questionnaires, in addition to the usual clinical data: * Hospital Anxiety and Depression scale (HAD) questionnaire, * Quality of life questionnaire EQ-5D-5L, * Brief Pain Inventory - French version: Questionnaire Concis de la Douleur (QCD), * Functional Impotence Scale for Low Back Pain: The Quebec Back Pain Disability Scale * Clinical Global Impression of Change (CGI-C)

Study details

Official title
Relevance of the Combined Extension-rotation-lateral Tilt Maneuver in the Selection of Patients With Chronic Low Back Pain for Neurotnomy Intervention Radiofrequency : Pilot Study
Conditions
Sponsor
FondationbHopale
Start date
2022-11-21
Primary completion
2023-11-15
Sex
All
Age range
from 18 Years to 65 Years
Results posted
No results posted in this snapshot
Countries
France
Total sites listed
1

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * Patients admitted to the chronic pain service at the Calot Institute with chronic low back pain for at least three months, not responding to well-conducted conservative treatment * Age 18 - 65 years * Patient did not object to the use of their data * Patient affiliated to a social security plan Non inclusion Criteria: * Patient with a disorder of hemostasis * Patient with a history of arthrodesis * Patient with radiologically visible root damage * Patient with instability of the spine * Patient with an abnormality on dorso-lumbar MRI: MODIC 1 * Patient under legal protection : * Person under guardianship, * Person under curatorship, * Person under legal protection, * Person deprived of liberty, * Pregnant or breastfeeding woman

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT05624307