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

Lumbar Disc Disease Clinical Trial

Official title:
Pilot Study to Assess the Efficacy of the ATLAS Medical Device on Pain in Patients With Subacute or Chronic Low Back Pain With Lumbar Disc Disease: Prospective, Randomized Trial (AmbuTract)

Clinical Trial 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.

Clinical Trial Description

The main expected benefit is a reduction in pain experienced in patients with subacute or chronic low back pain during and after wear. Consequently, an improvement in the quality of daily life is expected with a less significant impact of low back pain. The main objective of the study is to compare the efficacy of the ATLAS medical device with a standard lumbar support belt in terms of immediate reduction of low back pain experienced in patients with subacute or chronic low back pain. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04585386
Study type Interventional
Source GCS Ramsay Santé pour l'Enseignement et la Recherche
Contact
Status Terminated
Phase N/A
Start date August 18, 2021
Completion date October 7, 2021
View Details
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