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NCT06331507 Clinical Trial

Refinement and Assessment of New MRI Technologies for Cardiovascular Exams Using the Phillips CMR Patch

Cardiomyopathies Clinical Trial

Official title:
Refinement and Assessment of New MRI Technologies for Cardiovascular Exams Using the Phillips Cardiac Magnetic Resonance (CMR) Patch

Clinical Trial Details — Status: Terminated

Administrative data
NCT number NCT06331507
Other study ID # HUM00176904
Secondary ID
Status Terminated
Phase N/A
First received
Last updated
Start date September 2, 2021
Est. completion date June 29, 2023

Study information
Verified date March 2024
Source University of Michigan
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study is being done to improve image quality and provide the collaborator with feedback on wide band imaging in patients with cardiac implantable electronic devices (CIED).

Recruitment information / eligibility
Status Terminated
Enrollment 292
Est. completion date June 29, 2023
Est. primary completion date June 29, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: have a clinically ordered cardiac MRI exam at University of Michigan - Exclusion Criteria: pregnant; contraindication to MRI -

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• CMR patch
The Cardiac Magnetic Resonance (MR) patch is a sequence modification for enhancing the images in patients with devices (CIED) for assessing heart muscle scar. The Philips tested patch supports multiple cardiac MR imaging enhancements compiled from several individual patches generated by multiple Philips MR research collaborators for use on 1.5 Tesla Philips scanners.

Locations
Country Name City State
United States Michigan Medicine - University of Michigan Ann Arbor Michigan

Sponsors (2)
Lead Sponsor Collaborator
University of Michigan Philips Health Care

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Scan speed: Scan speed is time required to set-up and run the new technique relative to the standard method. Up to an hour
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