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Clinical Trials/NCT02874209
NCT02874209
Unknown
Not Applicable

Noninvasive Assessment of Neuronal Damage by MRI Sodium ( 23Na ) in Amyotrophic Lateral Sclerosis

Assistance Publique Hopitaux De Marseille1 site in 1 country60 target enrollmentSeptember 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Amyotrophic Lateral Sclerosis
Sponsor
Assistance Publique Hopitaux De Marseille
Enrollment
60
Locations
1
Primary Endpoint
Central conduction time of the potential muscle through transcranial magnetic stimulation
Last Updated
9 years ago

Overview

Brief Summary

Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease affecting the central and peripheral motor neurons, characterized by the rapidity of its evolution (median survival of 3 years). The pathophysiology of the disease is still poorly understood. Neuronal death results from several cellular mechanisms entangled, including mitochondrial dysfunction. The absence of diagnostic marker causes a significant delay in diagnosis, on average a year. On the other hand, the wish biomarker is important for therapeutic trials. Recently, MRI sodium (23Na) demonstrated its importance to detect noninvasively sodium accumulations associated with neuronal suffering. This neuronal pain can be caused by mitochondrial dysfunction causing the accumulation in the sodium and calcium cell causing neuronal death. These studies were conducted in multiple sclerosis, Alzheimer's disease, Huntington's disease, stroke and brain tumors. They demonstrated that sodium MRI could be an effective and sensitive biomarker for detecting and quantifying neuronal degeneration. The goal of this study is to assess neuronal damage noninvasively by MRI sodium in amyotrophic lateral sclerosis.

Registry
clinicaltrials.gov
Start Date
September 2015
End Date
September 2018
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Amyotrophic lateral sclerosis patient according to the El Escorial criteria revised Brooks et al. 2000 bulbar or spinal beginning

Exclusion Criteria

  • patient or healthy volonteer presenting MRI contre indications to this exam.
  • patient or healthy volonteer presenting severe high blood pressure undergoing medication to treat it or not.
  • patient or healthy volonteer having chronic psychiatric illness, dementia

Outcomes

Primary Outcomes

Central conduction time of the potential muscle through transcranial magnetic stimulation

Time Frame: 4 hours

Study Sites (1)

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