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ETNA-MS Device Validation Study — ETNA-MS  

Multiple Sclerosis Clinical Trial

Official title:
ETNA-MS Device Validation Study

Clinical Trial Summary

The overarching goal of this research protocol is to validate the effectiveness of Innodem's ETNA-MS device in informing clinicians on the disability status of Multiple Sclerosis (MS) patients. Effectiveness of the device will be assessed by the level of agreement between the EDSS estimated by the device and the actual scores measured by the neurologist in-person assessments.

Clinical Trial Description

This study will use a multi-site cross-sectional design in a single cohort of Multiple Sclerosis (MS) patients. Eligible patients with MS will be selected and categorized based on their Expanded Disability Status Scale (EDSS) score. Patients eye movements will be captured using the patented eye-tracking technology at one single time point. In addition to the eye-tracking tests, patient phenotypes will be further detailed via brief functional and cognitive assessments using the EDSS, Brief International Cognitive Assessment for MS (BICAMS) and Multiple Sclerosis Functional Composite (MSFC). All patients will be required to participate in a single session. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06256731
Study type Observational [Patient Registry]
Source Innodem Neurosciences
Contact
Status Recruiting
Phase
Start date December 12, 2023
Completion date June 12, 2024
View Details
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