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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT02047396
Other study ID # 13-009187
Secondary ID R01HL136659
Status Active, not recruiting
Phase
First received
Last updated
Start date January 2014
Est. completion date January 2025

Study information

Verified date April 2024
Source Mayo Clinic
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

To comprehensively characterize Left Ventricular (LV) remodeling after Myocardial Infarction (MI) in the community, study the association between patterns of remodeling and biological pathways and examine the association between the predictors of remodeling and heart failure after Myocardial Infarction.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 1599
Est. completion date January 2025
Est. primary completion date August 31, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: 1. Hospitalized patients with a clinical diagnosis of Myocardial Infarction. 2. Residents of Olmsted, Dodge, Goodhue, Wabasha, Winona, Fillmore and Mower Counties. 3. Able to provide informed consent. Exclusion Criteria: 1. Previous clinical diagnosis of Myocardial Infarction 2. Previous diagnosis of Heart Failure and/or Cardiomyopathy 3. Diagnosis of Apical Ballooning Syndrome 4. Planned Coronary Artery Bypass Graft (CABG) during index hospitalization 5. Unable to provide informed consent

Study Design


Locations

Country Name City State
United States Mayo Clinic Rochester Minnesota

Sponsors (2)

Lead Sponsor Collaborator
Mayo Clinic National Heart, Lung, and Blood Institute (NHLBI)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Heart Failure Development of Heart Failure post Myocardial Infarction 5 years
Secondary Death All cause mortality post Myocardial Infarction 5 years
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