Actively Recruiting
Glucose Consumption in MS Using [F-18]FDG-PET
Led by Brigham and Women's Hospital · Updated on 2026-01-09
50
Participants Needed
1
Research Sites
134 weeks
Total Duration
On this page
Sponsors
B
Brigham and Women's Hospital
Lead Sponsor
G
Genzyme, a Sanofi Company
Collaborating Sponsor
AI-Summary
What this Trial Is About
Given the need for better diagnostic imaging techniques in multiple sclerosis (MS), the study aims to investigate the utility of \[F-18\]FDG positron emission tomography (PET) in MS. The study will be assessing glucose consumption patterns in subjects with progressive MS (PMS) and relapsing-remitting MS (RRMS), as well as healthy controls. PET will be compared to magnetic resonance imaging (MRI) lesion load and brain atrophy, and serum and blood biomarkers, as well as clinical measures of physical disability, cognitive impairment, fatigue, and depression. This study's findings may pave a path for integrating \[F-18\]FDG-PET in routine clinical practice for MS, improving patient experiences and outcomes. The specific aims of the study are: Aim 1: To compare glucose consumption in the brain in subjects with PMS, relapsing-remitting MS (RRMS), and healthy controls, using the radiolabeled glucose analogue 18-fluorodeoxyglucose, also known as \[F-18\]FDG. Aim 2: To compare the relationship between FDG-PET and standard 3T MRI measures including global and regional brain atrophy and lesion load, and to compare FDG-PET with MRI in terms of their relationship with clinical measures of physical disability, cognitive impairment, fatigue and depression in MS subjects. Aim 3: To assess the relationship of FDG-PET with serum and blood biomarkers, including but not limited to sNfL, GFAP, IL-6, and TNFα in MS.
CONDITIONS
Official Title
Glucose Consumption in MS Using [F-18]FDG-PET
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 to 70 years
- Diagnosed with multiple sclerosis (including secondary progressive, relapsing-remitting, or primary progressive) by International Panel Criteria
- Age and sex-matched healthy controls also eligible
- Willing to undergo PET and MRI imaging
- Able to provide informed consent
You will not qualify if you...
- Known alternate neurological disorders, previous head injury, or substance abuse
- Known neuropsychiatric disorders including bipolar disease and schizophrenia
- Medical conditions that prevent study procedures
- Women who are pregnant, nursing, seeking pregnancy, or suspect pregnancy
- Claustrophobia
- Non-MRI compatible implanted devices
- Corticosteroid treatment within the past four weeks
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Brigham & Women's Hospital
Boston, Massachusetts, United States, 02115
Actively Recruiting
Research Team
N
Nicolas Horan
CONTACT
S
Steven Cicero
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
DIAGNOSTIC
Number of Arms
1
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