Clinical Trial

Low-Field MRI in Stroke Code Patients

Study acronym: LFMIS
Recruiting
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Summary
This study evaluates the accuracy and feasibility of a portable low-field MRI (Hyperfine) device in patients presenting to the emergency department with suspected acute stroke. All enrolled patients undergo standard clinical imaging (CT, CT angiography, CT perfusion) and additionally receive a low-field MRI scan. Low-field MRI findings are compared to routine CT imaging and final clinical diagnosis. The study aims to determine whether low-field MRI can reliably detect acute ischemic stroke (including lacunar and large vessel occlusion), hemorrhagic stroke, and stroke mimics in the acute setting. Secondary outcomes include feasibility measures such as scan time, completion rate, patient satisfaction, and adverse events.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2026-07-10.
Trial Details
NCT Number NCT07702968
Lead Sponsor Leiden University Medical Center
Conditions Acute Stroke, MRI Imaging
Enrollment 80 participants
Start Date 2026-04-20
Primary Completion 2027-04-01 (estimated)
Study Completion 2027-08-01 (estimated)
Updated on ClinicalTrials.gov 2026-07-16