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Imaging and Blood Tests to Track Amyotrophic Lateral Sclerosis Over Time

Studies brain and spine scans and blood tests in adults with ALS and healthy people.

Plain-language title generated from the registry record
Registry title: Multicenter ALS Imaging Study

Key facts

Where
Evanston, Gainesville, and Minneapolis, United StatesSee the 3 sites

Where in United States

  • Northwestern UniversityEvanston, United StatesTaking people
  • University of FloridaGainesville, United StatesTaking people
  • University of MinnesotaMinneapolis, United StatesTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
University of Minnesota
Trial code
NCT06735014
Record updated
31 July 2026
Original description
This is a multi-site study of ALS participants and healthy controls who will undergo brain and cervical spine MRIs and NfL blood testing at up-to 4 time points over the course of a year. The primary goal is to identify objective biomarkers of disease progression that are biologically relevant, linearly progressive, and sensitive to change.Read full original descriptionShow less

Multicenter Longitudinal Imaging in ALS for Disease Biomarker Development

This is a multi-site study of ALS participants and healthy controls who will undergo brain and cervical spine MRIs and NfL blood testing at up-to 4 time points over the course of a year. The primary goal is to identify objective biomarkers of disease progression that are biologically relevant, linearly progressive, and sensitive to change.

Exclusion: Individuals will be excluded if they have any condition that makes MRI unsafe or if they are unable to comply with instructions; All participants will undergo a neurologic examination at enrollment. Control participants with clinically significant abnormal findings on neurological examination will be excluded from the study.

For participants with ALS:; < 36 months since onset of symptoms; Definite, probable, lab-supported probable, or possible ALS by El Escorial criteria OR definite, probable, or possible ALS per Awaji-Shima criteria OR meets Gold Coast criteria; Forced vital capacity within the last 90 days ≥ 60% of the predicted value; Able to consent for themselves; Able to read and speak English; Clear of any contraindications for MRI.

ClinicalTrials.gov NCT06735014