Informations générales (source: ClinicalTrials.gov)

NCT04785001 En recrutement IDF
Assessment of New Physiological, Radiological and Activity Markers in Patients Treated by Spinal Cord Stimulation for Chronic Lower Limb Pain
Observational
Fondation Ophtalmologique Adolphe de Rothschild (Voir sur ClinicalTrials)
juillet 2021
septembre 2024
29 juin 2024
By combining the usual care of patients eligible for spinal cord stimulation (SME) with measurements of the HRV index (Heart Rate Variability), objective measurements of activity (number of steps, quality of sleep) and measurements of connectivity obtained by anatomical and functional magnetic resonance imaging (fMRI), the collection of preliminary data necessary for the analysis of markers correlated with the efficiency of stimulation will be possible. Ultimately, these markers could be used to optimize the perioperative management of these patients.
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Etablissements

Les établissements d'Île-de-France ayant mis à jour leurs données Origine et niveau de fiabilité des données
HOPITAL FONDATION A. DE ROTHSCHILD Hayat BELAID En recrutement IDF 21/06/2024 13:33:22  Contacter

Critères

Tous
Inclusion Criteria:

- Lower limb pain included in the inclusion criteria for spinal cord stimulation
according to HAS recommendations: neuropathic, lumbar radicular sequelae after
spinal surgery, complex regional pain syndrome (CRPS)

- Chronic pain that has been present for at least 6 months

- Rebellious pain resistant to drug and non-drug treatments well conducted;

- Functional impact defined by a score> 20% on the Oswestry scale;

- Patient affiliated or beneficiary of a social security scheme;

- Patient who consented to participate in the study.



- Presence of a surgical contraindication to the implantation of material (chronic
infection, long-term anticoagulant treatment that cannot be interrupted,
contraindication to anesthesia);

- Addiction (according to DSM IV);

- Major depressive syndrome despite appropriate treatment and / or psychotic symptoms
(according to DSM IV);

- Unbalanced psychiatric disorder;

- Intermittent pain or present for less than 6 months;

- Diffuse painful syndrome;

- Progressive disease, associated inflammatory rheumatic pathology, and any other
disabling pathology limiting physical activity (advanced articular osteoarthritis);

- Absolute contraindication to MRI (e.g. pace-maker, implantable stimulator,
intra-orbital metallic foreign body);

- Language barrier or cognitive disorders preventing understanding of the research
protocol;

- Person benefiting from a legal protection measure;

- Pregnant or breastfeeding woman.