A quick 10-minute heart scan for cardiac diseases

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study focuses on developing a new 10-minute cardiovascular magnetic resonance (CMR) protocol aimed at improving diagnostic capabilities for various cardiac conditions without the need for contrast agents. The protocol is designed to standardize assessments for approximately 70% of cardiac patients by evaluating heart function and myocardial tissue characteristics. The study will assess the clinical feasibility, performance, and cost-effectiveness of this approach across different populations, including those with non-ischemic cardiomyopathies and ischemic heart disease.

Why it matters

Who can join: the full rules

Healthy Volunteers

Inclusion Criteria:

* Age: \> 18y, Informed consent No known current or pre-existing significant medical conditions that would affect the cardiovascular or respiratory system

Exclusion Criteria:

* General MRI contraindications: MR- incompatible devices such as pacemakers, defibrillators, or implanted material or foreign bodies. 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

Patients

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

Where it's running

• McGill University Health Center
  Montreal, Quebec, Canada Recruiting

Study contacts

• Principal investigator: Matthias G Friedrich, MD — McGill University Health Centre/Research Institute of the McGill University Health Centre
• Study coordinator: Elizabeth Konidis
• Email: elisavet.konidis@muhc.mcgill.ca
• Phone: 514-934-1934

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.