Ventricular Remodeling and Heart Failure After Myocardial Infarction: A Community Study
2 other identifiers
observational
1,599
1 country
1
Brief 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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jan 2014
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2014
CompletedFirst Submitted
Initial submission to the registry
January 23, 2014
CompletedFirst Posted
Study publicly available on registry
January 28, 2014
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 31, 2018
CompletedStudy Completion
Last participant's last visit for all outcomes
January 1, 2030
ExpectedFebruary 23, 2026
February 1, 2026
4.7 years
January 23, 2014
February 19, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
Heart Failure
Development of Heart Failure post Myocardial Infarction
5 years
Secondary Outcomes (1)
Death
5 years
Study Arms (1)
Myocardial Infarction subjects
Subjects with first Myocardial Infarction presenting to one of the Mayo Clinic Hospitals in Rochester, Minnesota.
Eligibility Criteria
Subjects in the 7 County area who are admitted to the Mayo Clinic Hospitals in Rochester, Minnesota who have their first myocardial infarction and are willing to have blood drawn and return for an echocardiogram in 3 months.
You may qualify if:
- Hospitalized patients with a clinical diagnosis of Myocardial Infarction.
- Residents of Olmsted, Dodge, Goodhue, Wabasha, Winona, Fillmore and Mower Counties.
- Able to provide informed consent.
You may not qualify if:
- Previous clinical diagnosis of Myocardial Infarction
- Previous diagnosis of Heart Failure and/or Cardiomyopathy
- Diagnosis of Apical Ballooning Syndrome
- Planned Coronary Artery Bypass Graft (CABG) during index hospitalization
- Unable to provide informed consent
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Mayo Cliniclead
- National Heart, Lung, and Blood Institute (NHLBI)collaborator
Study Sites (1)
Mayo Clinic
Rochester, Minnesota, 55905, United States
Biospecimen
Plasma, serum, and WBCs
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Suzette Bielinski, PhD
Mayo Clinic
Study Design
- Study Type
- observational
- Observational Model
- ECOLOGIC OR COMMUNITY
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
January 23, 2014
First Posted
January 28, 2014
Study Start
January 1, 2014
Primary Completion
August 31, 2018
Study Completion (Estimated)
January 1, 2030
Last Updated
February 23, 2026
Record last verified: 2026-02
Data Sharing
- IPD Sharing
- Will not share