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Search / Trial NCT03050346

Trial Information

Current as of April 26, 2025

Completed

Keywords

Magnetic Resonance Imaging Coronary Artery Disease Apnea Hyperventilation Bold Breathing Maneuvers Myocardial Oxygenation

ClinConnect Summary

This is a clinical trial to test the clinical feasibility and safety of a novel CMR protocol. It aims to investigate a new Cardiovascular Magnetic Resonance (CMR) technique, called oxygenation-sensitive CMR (OS-CMR).

OS-CMR is a T2\*-sensitive CMR sequence based on the so-called blood-oxygen-level-dependent (BOLD) effect. Because de-oxygenated hemoglobin acts as an endogenous paramagnetic contrast agent, the signal intensity (SI) in OS-CMR images is linearly correlated with hemoglobin oxygenation in the tissue. An increase in deoxyhemoglobin results in an drop in SI in OS-CMR images, while...

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Age \> 18 y
  • Informed consent as documented by signature (Appendix Informed Consent Form)
  • Indication for invasive coronary angiography based on symptoms and a test positive for inducible coronary ischemia
  • One-vessel or two-vessel CAD at coronary angiography (For healthy volunteers: absence of current or pre-existing cardiovascular and lung disease and absence of medication with cardiovascular effects)
  • Exclusion Criteria:
  • General MRI contraindications (i.e pacemakers, defibrillating wires, implanted defibrillators, intracranial aneurysm clips, metallic foreign bodies in the eyes, knowledge or suspicion of pregnancy)
  • Acute Coronary Syndrome (ACS) or other acute cardiac injury within 4 weeks
  • Previous myocardial infarction, percutaneous coronary intervention or coronary artery bypass surgery
  • Hemodynamically unstable conditions
  • Significant or uncontrolled arrhythmias
  • Lack of ability to follow commands
  • Vasoactive medication (e.g. nitro or ß blockers) or nutrition with caffeine (coffee, tea, cocoa, chocolate, "energy drink") during the 12 h before the exam
  • Non-ischemic cardiomyopathy
  • Severe Pulmonary Disease

About Mcgill University Health Centre/Research Institute Of The Mcgill University Health Centre

The McGill University Health Centre (MUHC) and the Research Institute of the McGill University Health Centre (RI-MUHC) are leading institutions in clinical research and healthcare innovation. With a commitment to advancing medical knowledge and improving patient outcomes, the MUHC integrates cutting-edge research with high-quality patient care. The RI-MUHC fosters a collaborative environment where multidisciplinary teams engage in transformative research across various fields, including oncology, neurology, and cardiovascular health. By leveraging state-of-the-art facilities and a robust network of clinical expertise, both entities strive to translate scientific discoveries into effective treatments, ultimately enhancing the quality of life for patients locally and globally.

Locations

Madison, Wisconsin, United States

Montreal, Quebec, Canada

Heidelberg, , Germany

Cape Town, , South Africa

Montreal, Quebec, Canada

Montreal, Quebec, Canada

London, , United Kingdom

Patients applied

0 patients applied

Trial Officials

Matthias Friedrich, MD

Principal Investigator

McGill University Health Centre/Research Institute of the McGill University Health Centre

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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