Low Field Magnetic Resonance Imaging Assessment With Outpatients

ConditionConditions Requiring a Brain Magnetic Resonance Imaging, Head Computerized Tomography, or Head Ultrasound

Trial statusRecruiting

Trial phaseNot applicable

Trial typeInterventional

Biological sexAll

Age0-22

SponsorChildren's Mercy Hospital Kansas City

About this trial

The objective of the study is to perform imaging assessments of an early stage magnetic resonance imaging (MRI) system on patients using low field magnetic strength.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

None

Disqualifiers

None

Trial design

Design model

Single group

Treatments tested in this trial

Hyperfine MRI
Diagnostic test
Patients who have a standard of care MRI, CT or US will undergo a low-field MRI utilizing Hyperfine either at the patient's bedside or in the department of Radiology. Results of the Hyperfine MRI will not be used for clinical care and will only be available to members of the research team for review.

Treatment groups

500 Participants

are divided into 1 treatment group

Group A: HyperfineExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

Sensitivity and specificity of hyperfine MRI versus conventional MRI, CT and/or US

Time frame

Through study completion, an average of 3 years

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Children's Mercy Hospital Kansas City

Lead sponsor

Source ClinicalTrials.gov

Apply now