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Clinical Trials/NCT01821924
NCT01821924
Completed
Not Applicable

Role of Stress CMR in Predicting Adverse Clinical Events in Patients With Known or Suspected Ischemic Heart Disease

Brigham and Women's Hospital2 sites in 1 country2,347 target enrollmentJanuary 30, 2012

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Coronary Artery Disease
Sponsor
Brigham and Women's Hospital
Enrollment
2347
Locations
2
Primary Endpoint
A composite outcome measure consisting of cardiovascular mortality and nonfatal MI after index CMR.
Status
Completed
Last Updated
5 months ago

Overview

Brief Summary

The investigators plan to use retrospective data to assess heart function and structure abnormalities through the use of an approved vasodilating agent for stress cardiac MRI tests. The investigators are interested in how these MRI findings relate to long-term prognosis in people who are at risk for cardiac disease.

Registry
clinicaltrials.gov
Start Date
January 30, 2012
End Date
August 30, 2018
Last Updated
5 months ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Raymond Y. Kwong, MD

Principal Investigator

Brigham and Women's Hospital

Eligibility Criteria

Inclusion Criteria

  • Age \>/= 21 years old
  • No contraindications for cardiac MRI (by renal function or metallic hazards)

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

A composite outcome measure consisting of cardiovascular mortality and nonfatal MI after index CMR.

Time Frame: target follow up of at least 4 years

"Myocardial infarction" will be defined as hospital admission for acute coronary syndrome (defined by positive serum troponin level with documented electrocardiographic changes, clinical syndrome, or need for percutaneous or surgical revascularization).

Secondary Outcomes

  • A composite outcome measure consisting of cardiovascular mortality, nonfatal MI, hospitalization for unstable angina or congestive heart failure, and late unplanned coronary bypass surgery at at least 6 months after index CMR.(target follow up of at least 4 years)

Study Sites (2)

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