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Recruiting Observational

EIM Via the Myolex mScan as an ALS Biomarker

NCT06491732 · tracked via the Priya Life Science Israel tracker
Phase
Observational
Started
2025-03-01
Last updated
2026-04-22

Condition(s) studied

Amyotrophic Lateral Sclerosis

Investigational drug(s) / intervention(s)

Electrical Impedance Myography

Electrical Impedance Myography: EIM is an impedance-based technology in which an imperceptible, high-, multi-frequency (e.g., 1 kHz to 10 MHz) electrical current is applied across two electrodes; the resulting voltage signals are measured across two sense electrodes

Study summary

Amyotrophic lateral sclerosis (ALS) has been traditionally considered incurable and untreatable. But starting in the 1990s with the introduction of Riluzole, therapies are being discovered and ultimately approved for slowing disease progression. Many pharmaceutical companies continue to seek new therapeutic approaches. One critical aspect of all clinical trials is the need track to progression sensitively to identify the impact of therapy. Tools to track ALS progression must be convenient, objective, require minimal training, be easily standardized, cost-efficient, and have the potential to be applied effectively at home. There has been a push to identify accurate, objective biomarkers of ALS progression. In this study, the investigators propose to use Electrical impedance myography (EIM) to evaluate the progression of the disease. Work has shown that the EIM 50 kilohertz (kHz) phase value from one or more muscles, followed sequentially, can serve as an effective overall biomarker for assessing the rate of ALS progression for a single person.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Sporadic or familial ALS diagnosed as clinically possible, probable, lab-supported probable, or definite ALS defined by revised El Escorial criteria * Capable of providing informed consent and complying with study procedures in the investigator's opinion * Time since ALS symptom onset ≤36 months * Vital Capacity of ≥40% of predicted capacity as measured by forced vital capacity or slow vital capacity * Must have a study partner for home visits * Access to the internet for data upload * Age 18 years or older Exclusion Criteria: * Clinically significant unstable medical condition (other than ALS) that would affect the participant's ability to participate, according to the investigator's judgment * Patient with pure upper motor neuron disease (PLS) * Known history of unstable psychiatric disease, cognitive impairment, dementia, or active substance abuse * Significant pitting edema (2+ or more) that would interfere with EIM measures * Active cancer or history of cancer treated with chemotherapy and/or radiation * BMI \>35

Primary outcome measure(s)

  • EIM phase change over time — 8 months
    Mean and standard deviation in rate of change in EIM phase values compared to mean and standard deviation in rate of change in ALSFRS-R over 8 months

Trial sites (6)

FacilityCityRegionStatus
Barrow Neurological Institute Phoenix Arizona Recruiting
Massachusetts General Hospital Boston Massachusetts Recruiting
Beth Israel Deaconess Medical Center Boston Massachusetts Recruiting
University of Michigan Ann Arbor Michigan Recruiting
Dartmouth Hitchcock Medical Center Lebanon New Hampshire Recruiting
Atrium Health Wake Forest Baptist Medical Center Winston-Salem North Carolina Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06491732 on ClinicalTrials.gov ↗ ← All trials in Israel