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Efficacy of the ATLAS Medical Device on Pain in Patients With Low Back Pain Due to Lumbar Disc Disease

NCT04585386 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 3

Last updated 2022-06-23

No results posted yet for this study

Summary

Monocentric, comparative, randomized, controlled interventionnal study in 2 parallel groups, aiming to compare the efficacy of the ATLAS device with that of a standard lumbar belt on the reduction of pain felt in patients with subacute or chronic low back pain with lumbar disc disease.

Conditions

  • Lumbar Disc Disease

Interventions

OTHER

Visual analog scale

to measure the lumbar and radicular pain felt by the patient.

OTHER

Mac Gill Pain Questionnaire

self-questionnaire that allows a qualitative assessment of chronic pain

OTHER

Roland and Morris Disability Questionnaire

functional disability scale for assessing low back pain

OTHER

Quebec questionnaire

To access the patient's perception of incapacity

Sponsors & Collaborators

  • GCS Ramsay Santé pour l'Enseignement et la Recherche

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-08-18
Primary Completion
2021-10-07
Completion
2021-10-07

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04585386 on ClinicalTrials.gov