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Clinical Trial Summary

Vertebral osteomyelitis is an infection of the intervertebral disk and adjacent vertebral plates with a non-negligible risk of neurological complications and handicap. If there are clear recommendations dealing with antibiotic therapy and surgery indications for this pathogen, the question of the immobilization will be remaining debate. The aim of the study was to describe protocols and practices for the immobilization of vertebral osteomyelitis in different French hospitals and bone and joint infections Centers. The secondary objectives were to evaluate the frequency of neurological complications in a large prospective cohort, and to identify clinical and imaging risk factors for neurological complications. The investigators also aim to search for association between type and duration of spine immobilization and neurological status at the end of follow-up.


Clinical Trial Description

Study design is descriptive, prospective, multicentric, and the investigators have a single database centralized in Nantes University Hospital. Patient's data will be conserved and trapped anonymously and patients all give oral consent. Information letter is given to each patient. Typical study calendar : Baseline : - Patient information (letter and oral consent) - Clinical data and comorbidities collection - Neurological examination - Spine X-ray - MRI or CT-scan imaging to confirm diagnosis During Hospitalization - Date collection : spine immobilization modalities (type, duration, changes…), duration of bed rest - Other treatments (antibiotic therapy : molecules and duration) - Daily neurological examination 3 months follow-up visit : (if usually done by physician) - Clinical and neurological examination - Spine immobilization assessment - Spine X-ray - Oswestry questionary 6 months follow-up visit : finale visit (if usually done by physician) - Clinical and neurological examination - Spine immobilization assessment - Spine X-ray - Oswestry questionary ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04655950
Study type Observational [Patient Registry]
Source Nantes University Hospital
Contact
Status Completed
Phase
Start date February 11, 2016
Completion date May 31, 2019

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