A 10-Minute Cardiovascular Magnetic Resonance Protocol for Cardiac Disease

  • STATUS
    Recruiting
  • days left to enroll
    40
  • participants needed
    2130
  • sponsor
    McGill University Health Centre/Research Institute of the McGill University Health Centre
Updated on 19 February 2024
heart disease
MRI
a 10
respiratory system

Summary

This study aims to identify and assess new CMR techniques that can improve current CMR protocols.

Description

The aim of this study is to develop a comprehensive 10-minute protocol based on function and myocardial tissue characterization without the need for contrast injection, which can be standardized for 70% of cardiac patients.

To test this 10-minute CMR protocol for its ability to significantly improve diagnostic decision-making and to reduce cost.

To test its clinical feasibility, performance and cost-effectiveness in different populations including: Non-ischemic cardiomyopathies (-)OS-CMR and Ischemic Heart Disease and CAD (+)OS-CMR

Details
Condition Aortic Regurgitation, Coronary Artery Disease, Coronary Artery Disease, Aortic Stenosis, Coronary heart disease, Vascular anomaly, Heart disease, Heart disease, VALVULAR HEART DISEASE, Dilated cardiomyopathy, Hypertrophic Cardiomyopathy, Pericardial effusion, Cardiomyopathy, Cardiomyopathy, Myocarditis, Congenital Heart Disease, Infiltrative Cardiomyopathy
Age 18years - 100years
Clinical Study IdentifierNCT04464655
SponsorMcGill University Health Centre/Research Institute of the McGill University Health Centre
Last Modified on19 February 2024

Eligibility

Yes No Not Sure

Inclusion Criteria

Age: >18 y, Informed consent, Clinically indicated CMR exam

Exclusion Criteria

General MRI contraindications: MR- incompatible devices such as pacemakers, defibrillators, or implanted material or foreign bodies Vasoactive medication (e.g. nitro) during the 12 hours prior to the exam. Consumption of caffeinated drinks or foods (including cocoa and chocolate) during the 12 hours prior to the exam
Regular nicotine consumption during the last 6 months
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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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