ClinConnect ClinConnect Logo
Search / Trial NCT06089486

MARINER Trial: Multiparametric Cardiac PET for CAV Surveillance After Heart Transplantation

Launched by OTTAWA HEART INSTITUTE RESEARCH CORPORATION · Oct 12, 2023

Trial Information

Current as of June 26, 2025

Recruiting

Keywords

Heart Transplant

ClinConnect Summary

The MARINER Trial is studying a new way to monitor heart transplant patients for a condition called cardiac allograft vasculopathy (CAV), which happens when the blood vessels in the transplanted heart become narrow and can lead to problems with how the heart functions. This trial aims to find out if a noninvasive imaging technique called positron emission tomography (PET) is just as effective as the traditional method known as coronary angiography, which is a more invasive procedure that involves threading a catheter through the blood vessels.

To participate in this trial, you need to be at least 18 years old and have had a heart transplant between 2 to 10 years ago. You should also be able to give informed consent, meaning you understand what the trial involves. However, certain health conditions may prevent you from joining, such as severe heart issues or allergies to specific contrast dyes used in imaging. If you participate, you'll undergo the PET scan and may be closely monitored to see how well this method works for checking your heart's health compared to the standard procedure. This trial is currently recruiting participants, and it offers a chance to help improve care for future heart transplant patients.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • 1. Post heart transplant 2-10 years.
  • 2. Age ≥18 years.
  • 3. Able to provide informed consent.
  • Exclusion Criteria:
  • 1. Contraindication to dipyridamole due to severe aortic stenosis.
  • 2. Contraindication to dipyridamole due to 2:1 or greater AV block without pacemaker.
  • 3. Contraindication to dipyridamole due to severe bronchospasm.
  • 4. Unable to undergo coronary angiography due to allergy to iodinated contrast.
  • 5. Unable to undergo coronary angiography due to glomerular filtration rate ≤30 mL/min/1.73 m2. for non-dialysis patients as determined by local laboratory analysis.
  • 6. Unable to undergo coronary angiography due to unsuitable vascular access.
  • 7. Treated rejection ≤1-month.
  • 8. Unstable angina or MI ≤7 days.

About Ottawa Heart Institute Research Corporation

The Ottawa Heart Institute Research Corporation is a leading clinical research organization dedicated to advancing cardiovascular medicine through innovative research and clinical trials. Affiliated with the renowned University of Ottawa Heart Institute, the corporation focuses on conducting high-quality, ethically-driven studies that aim to improve patient outcomes and enhance understanding of heart-related diseases. With a commitment to collaboration and excellence, the organization engages multidisciplinary teams of researchers, healthcare professionals, and industry partners to translate scientific discoveries into effective therapies and interventions for cardiovascular health.

Locations

Ottawa, Ontario, Canada

Montreal, Quebec, Canada

Calgary, Alberta, Canada

Edmonton, Alberta, Canada

Toronto, Ontario, Canada

Patients applied

0 patients applied

Trial Officials

Sharon Chih

Principal Investigator

Ottawa Heart Institute Research Corporation

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported