Image
Conditions
Keywords
MRI, Radiology
Brief summary
The purpose of this pilot study is to compare a standard of care MRI scan to a non-standard of care MR imaging with portable (0.064 Tesla) MRI following the administration of non-SOC contrast called Gadopiclenol on 10 subjects with known brain tumors. Participants will be randomized to receive either standard MRI or portable MRI first following contrast injection
Detailed description
This study compares a routine MRI scan with a new portable MRI scanner known as the Hyperfine using a contrast dye called Gadopiclenol, the contrast is FDA approved. If participants choose to participate in this study, they will receive two MRI scans on the same day. One on the traditional standard of care MRI scanner and the other on the new portable Hyperfine MRI. The Hyperfine MRI scanner is not FDA approved due to being a very low risk medical device. However, the device is compliant with all of the FDA requirements regarding design control regulations and risk analysis. Participants will only receive one contrast injection that will be used for both scans. The selection of which scan is given first will be randomly selected (50/50 chance). Participation in this study will last two days. The first day participants will receive both MRI scans and the second day participants will receive a phone call from the research staff to check on them.
Interventions
DRUGGadopiclenol
Subjects will receive Gadopiclenol instead of standard of care contrast
DEVICECE MRI on 0.064T Scanner
Pt will undergo contrast enhanced images using Gadopiclenol on Hyperfine MRI
Sponsors
Guerbet
Medical University of South Carolina
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Female or male adult patient (18 years and older). * Patient presenting, at the time of inclusion, with known or highly suspected focal areas of disrupted Blood Brain Barrier (BBB) due to primary or secondary tumor/s. This lesion must have been detected on a previous imaging procedure (computerized Tomography (CT) or MRI). * Patient scheduled for a routine CNS contrast-enhanced MRI examination for clinical reasons. * Patient able and willing to participate in the study. * Patient with health insurance.
Exclusion criteria
* Patient presenting with acute or chronic Grade III (at least) renal insufficiency, defined as an estimated Glomerular Filtration Rate (eGFR) \<60 mL/min/1.73m² based on eGFR assessment on the day of each MRI. * Pregnant or breast-feeding female patient (a female patient of childbearing potential must be using a medically approved contraception method until the last study visit). * Patient with any contraindication to MRI examinations including active implants, passive implants which are MRI incompatible, and metallic foreign bodies. * Patient with known contra-indication(s) to the use or with known sensitivity to any GBCA. * Patient having received any contrast agent (MRI or CT) within 3 days prior to study gadopiclenol administration
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Visibility of lesions | 1 Day | Visibility of lesions and diagnostic capabilities of 0.068T MRI |
Outcome results
None listed