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The purpose of this protocol is to test a new Electrical Impedance Myography (EIM) device and study its reliability and ability to differentiate ALS patients from healthy controls.
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Lead Sponsor
Skulpt, Inc.
Collaborators
NCT03233646 · Alzheimer's Disease, Mild Cognitive Impairment, and more
NCT07233148 · Amyotrophic Lateral Sclerosis (ALS), Motor Neuron Disease (MND), and more
NCT07187388 · Amyotrophic Lateral Sclerosis (ALS), Primary Lateral Sclerosis (PLS), and more
NCT07202494 · Multiple Sclerosis, Neuromyelitis Optica Spectrum Disorders, and more
NCT04244630 · Amyotrophic Lateral Sclerosis (ALS)
Convergence Medical Devices
Boston, Massachusetts
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This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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