RECRUITING

Novel MRI Biomarkers for Monitoring Disease Progression in ALS

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

Routine MRI is normal in motor neuron diseases such as ALS. However, advanced MRI techniques can provide an objective measure of degeneration (a "biomarker") by examining brain structure, wiring, chemistry, and function. We will develop and evaluate novel MRI techniques that could improve our understanding of ALS and provide a means to diagnose it sooner and monitor its progression. Importantly, we expect these techniques to improve how new drugs are tested, which may lead to the more rapid discovery of a treatment for ALS. Each participant will have 3 MRI scans over a period of 8 months, along with neurological and cognitive evaluations. Study visits will take 2 - 3 hours. MRI is a safe technique that does not involve radiation.

Official Title

Novel MRI Biomarkers for Monitoring Disease Progression in ALS

Quick Facts

Study Start:2016-10
Study Completion:2024-12-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT03362658

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Patients with a suspected or confirmed diagnosis as described in Study Populations
  2. * For those with a diagnosis of ALS, patients will be considered with an El Escorial classification of suspected, possible, probable, probable lab-supported, and definite ALS.
  3. * Patients 18 years of age or older
  4. * Healthy controls over the age of 40.
  5. * Be able to lie in an MRI machine for approximately 60 minutes
  1. * Subjects with psychiatric/CNS illnesses such as Major Depressive Disorder, Schizophrenia, and Bipolar disorder.
  2. * Subjects with significant head injury or other neurological disease (stroke, brain tumour).
  3. * Subjects ineligible for MRI investigation due to a pacemaker or other metallic foreign body.

Contacts and Locations

Study Contact

Sara Moradipoor, MSc
CONTACT
780-248-1805
moradipo@ualberta.ca

Principal Investigator

Sanjay Kalra, MD
PRINCIPAL_INVESTIGATOR
FRCPC

Study Locations (Sites)

University of Miami
Miami, Florida
United States
University of Utah
Salt Lake City, Utah, 84108
United States

Collaborators and Investigators

Sponsor: University of Alberta

  • Sanjay Kalra, MD, PRINCIPAL_INVESTIGATOR, FRCPC

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2016-10
Study Completion Date2024-12-31

Study Record Updates

Study Start Date2016-10
Study Completion Date2024-12-31

Terms related to this study

Keywords Provided by Researchers

  • Magnetic Resonance Imaging
  • MRI
  • Biomarker

Additional Relevant MeSH Terms

  • Amyotrophic Lateral Sclerosis
  • Motor Neuron Disease