Fact CheckerSign in

NCT04908306Completed

IMAGE-HF: Project IIa Canadian CArdiomyopathy Registry for Device Therapy

IMAGE-HF: Project IIa - Canadian CArdiomyopathy Registry for Device Therapy (CanCARD-MR)

Source: ClinicalTrials.gov · Last updated 13 May 2026

Brief summary (registry, in English)

Delayed enhanced MRI in patients (of either ischemic or non-ischemic cause) being referred for primary prevention ICD

Status (registry)
Completed
Study type
Observational
Enrollment
502 (actual)
First submitted
26 May 2021
Start date
11 Oct 2011
Primary completion date
12 Jul 2024
Lead sponsor
Ottawa Heart Institute Research Corporation
NCT number
NCT04908306

What you commit to

  • Study type: Observational
  • Participants enrolled: 502
  • From 11 Oct 2011 to the primary completion date, 12 Jul 2024
  • No sites listed in no country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Recent myocardial infarction or revascularization procedure within the past 3 months.

Lab values

  • GFR (glomerular filtration rate) ≤ 30 ml. / min/ m2.

Other

  • Known contra-indications to MRI.

Who the study is looking for

  • .Any patient accepted for primary prevention ICD (+/-) CRT)

Sex: All

Full criteria on ClinicalTrials.gov

This page is information, not medical advice. Discuss any trial with your doctor.