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NCT05204459Recruiting

MS-ResearchBiomarkerS

Investigating the Longitudinal Relationships Between Visual Pathway Injury, Radiological and Blood Biomarkers in Multiple Sclerosis and Related Disorders

Source: ClinicalTrials.gov · Last updated 6 Feb 2024 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

This study is being conducted to investigate risk factors for disability progression in Multiple Sclerosis and related disorders (MSRD). The primary goal is to assess whether combining information from visual assessment, blood markers, as well as historical and ongoing longitudinal MRIs of the brain, orbit (the part of the skull where eyes are located), and/or spinal cord can predict changes in quantitative disability measures related to MSRD and neurological disease.

Status (registry)
Recruiting
Study type
Observational
Enrollment
1000 (estimated)
First submitted
11 Jan 2022
Start date
11 Nov 2021
Primary completion date
11 Nov 2041
Lead sponsor
Cedars-Sinai Medical Center
NCT number
NCT05204459

What you commit to

  • Study type: Observational
  • Planned participants: 1000
  • From 11 Nov 2021 to the primary completion date, 11 Nov 2041
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Patients will be excluded from the MRI portions of the study if they have a contraindication to MRI(metallic implantsor foreign bodies, claustrophobia, MRI-incompatible pacemakers, MRI- incompatible prosthetic heart valves).

Age

  • Patients will be excluded from the visual assessment portions of the study if they have had any recent ocular surgery (within the past two months), refractive errors of greater than or equal to ±6 diopters or other eye diseases that may affect or confound OCT/OCTA measurements (ex., age-related macular degeneration, advanced geographic atrophy, diabetic retinopathy, glaucoma).

Other

  • Patients will be excluded from the MRI portions of the study if they are pregnant, but their demographic, clinical information,and disability measures may still be captured under the study.

Who the study is looking for

  • Subjects who meet any one of the following diagnostic criteria:
    • Diagnosis of MS, CIS,or RIS based on the 2017 revised McDonald criteria.
    • Diagnosis of NMOSD based on the 2015 revised NMOSD consensus diagnostic criteria.
    • Diagnosis of myelin oligodendrocyte glycoprotein (MOG)-related encephalomyelitis, optic neuritis, or other associated disease.
    • Diagnosis of neurological disorders other than MSRD.
    • Healthy volunteer.
  • Age ≥18.
  • Able to give informed consent.

Age in the registry: 18 years to - · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Cedars-Sinai Medical Center
Coordinator of this site? Confirm its status
Los AngelesUnited StatesRecruiting

Related publications

This page is information, not medical advice. Discuss any trial with your doctor.