Actively Recruiting

Age: 18Years +
All Genders
NCT06309862

Immune Checkpoint Inhibitor Therapy for Cancer and Risk of Myocarditis or Cardiomyopathy

Led by Sunnybrook Health Sciences Centre · Updated on 2024-06-07

15

Participants Needed

1

Research Sites

82 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Patients undergoing dual treatment with Immune checkpoint inhibitors (ICI) for various cancers, e.g. melanoma, are at increased risk of developing myocarditis and cardiomyopathy. Currently, only limited data on serial myocardial tissue changes during treatment and whether they predict outcomes are available. Cardiac MRI (CMR) is the reference standard for non-invasive myocardial volumes/function analysis and uniquely characterizes myocardial tissue. Therefore, it may help detect myocardial tissue changes during treatment and help early treatment and prevent adverse cardiac outcomes.

CONDITIONS

Official Title

Immune Checkpoint Inhibitor Therapy for Cancer and Risk of Myocarditis or Cardiomyopathy

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients 18 years of age or older with skin cancer eligible for treatment with nivolumab, pembrolizumab, or ipilimumab
  • Able to provide informed consent
  • Able to travel to the study site for cardiac imaging
Not Eligible

You will not qualify if you...

  • Life expectancy of 12 months or less
  • Currently participating in another clinical trial
  • Previous treatment with immune checkpoint inhibitors
  • History of cardiac disease such as heart failure, myocardial infarction, atrial fibrillation, or unstable angina
  • Pregnant
  • Impaired kidney function with GFR of 30 mL/min or less
  • Contraindications to MRI such as having a pacemaker

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Sunnybrook Health Sciences Center

Toronto, Ontario, Canada, M4N 3M5

Actively Recruiting

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Research Team

C

Christian Houbois, MD

CONTACT

N

Navpreet Sekhon, MB Bch BAO

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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