Low Field Magnetic Resonance Imaging Assessment With Outpatients

Children's Mercy Hospital Kansas City500 enrolled

Overview

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.

Study Type

INTERVENTIONAL

Allocation

Purpose

DIAGNOSTIC

Masking

NONE

Enrollment

500

Conditions

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

Interventions

Hyperfine MRIDIAGNOSTIC_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.

Eligibility

Sex: ALLMin age: 0 YearsMax age: 22 Years

Medical Language ↔ Plain English

Inclusion Criteria Outpatients at CMH Adele Hall Radiology ages 0 days to 22 years are eligible for enrollment. Exclusion Criteria No additional sedation will be given as part of this study and that sedation, if already administered, will not be altered for study purposes. Any patient who has a contraindication to having an MRI, such as: Non-MRI conditional implanted device or device that is not able to be removed for MRI examination

Locations (1)

Children's Mercy Kansas City

Kansas City, Missouri, United States

RECRUITING

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

Central Contacts

Maura Sien, MS, RT(R)

CONTACT

8163026065 mesien@cmh.edu

Sarah Foster

CONTACT

8162343273 ssfoster@cmh.edu

Data from ClinicalTrials.gov

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