Clinical Trials Directory

Trials / Completed

CompletedNCT04219969

FDG PET-MRI for the Diagnosis of Spinal Cord Lesions

Ideal Imaging Time Point Assessment for Spinal Cord Lesions of Unknown Etiology With FDG PET-MRI

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
11 (actual)
Sponsor
M.D. Anderson Cancer Center · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

To compare the results and understand the possible benefits from FDG-PET/MRI during different scanning time points after FDG, a type of contrast drug, is given.

Detailed description

Primary Objectives: --To identify the optimal imaging time point using F18-FDG positron emission tomography (PET) that gives the best lesion conspicuity as defined by the best lesion to background (L/B) ratio when evaluating spinal cord lesions of unknown etiology. Exploratory Objectives: * To identify malignancy specific factors in F18-FDG metabolism derived from metrics such as maximum standard uptake value (SUVmax), mean standard uptake value (SUVmean), total lesion glycolysis (TLG), metabolic tumor volume (MTV) and L/B ratio. * To identify patterns of metabolism derived from metrics such as SUVmax, SUVmean, TLG, MTV, L/B ratio and magnetic resonance imaging metrics such as regional perfusion abnormalities, apparent diffusion coefficient values and mean diffusivity measures. OUTLINE: Patients receive fludeoxyglucose F-18 intravenously (IV) over 1 minutes and then undergo PET-magnetic resonance imaging (MRI) over 15-60 minutes at 60, 300, and 480 minutes after fludeoxyglucose F-18 injection in the absence of unacceptable toxicity.

Conditions

Interventions

TypeNameDescription
DRUGFludeoxyglucose F-18Given IV
DEVICEMagnetic Resonance ImagingUndergo PET-MRI
PROCEDUREPositron Emission TomographyUndergo PET-MRI

Timeline

Start date
2018-09-21
Primary completion
2024-05-07
Completion
2024-05-07
First posted
2020-01-07
Last updated
2024-05-09

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT04219969. Inclusion in this directory is not an endorsement.