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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT04908306
Other study ID # 2011308-01
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date October 11, 2011
Est. completion date August 1, 2023

Study information

Verified date February 2023
Source Ottawa Heart Institute Research Corporation
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

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


Description:

Device therapy using defibrillators and cardiac resynchronization therapy (CRT) is an important advance in the care of patients with acquired heart disease and heart failure. In specific groups these devices appear to significantly reduce the risk of sudden cardiac death and progression of heart failure. However, our ability to identify ideal candidates, and those who are most likely to respond and benefit from this therapy, is poor. Preliminary studies using specialized Magnetic Resonance Imaging (MRI) appears to be one of the more valuable ways of predicting response to device therapy and holds substantial promise for patients with cardiomyopathy. Large, prospective registries are necessary to explore its real-world utility for risk prediction across a broad spectrum of patients. Can-CARD MR is a national, multi-centre registry designed to address this particular need.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 502
Est. completion date August 1, 2023
Est. primary completion date August 1, 2023
Accepts healthy volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - .Any patient accepted for primary prevention ICD (+/-) CRT) Exclusion Criteria: - Known contra-indications to MRI. - Recent myocardial infarction or revascularization procedure within the past 3 months. - GFR (glomerular filtration rate) = 30 ml. / min/ m2.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Ottawa Heart Institute Research Corporation

Outcome

Type Measure Description Time frame Safety issue
Primary Occurrence of a)appropriate ICD therapy (shock or anti-tachycardia pacing (ATP)) or sudden cardiac death Occurrence of a)appropriate ICD therapy (shock or anti-tachycardia pacing (ATP)) or sudden cardiac death 1 year
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