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Prospective Project to Identify Biomarkers of Morbidity and Mortality in Cardiovascular Interventional Patients

Cardiovascular Research Consortium - a Prospective Project to Identify Biomarkers of Morbidity and Mortality in Cardiovascular Interventional Patients

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03444259
Acronym
CAREBANK
Enrollment
1001
Registered
2018-02-23
Start date
2016-02-01
Completion date
2029-12-31
Last updated
2024-05-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Aortic Valve Disease, Aortic Valve Stenosis, Atrial Fibrillation, Cardiac Arrythmias, Cardiac Surgery, Cardiac Tumor, Coronary Artery Disease, Mitral Valve Disease

Keywords

Atrial fibrillation, Aortic stenosis, Coronary artery disease, Cardiac surgery, Atrial appendage

Brief summary

The objective of CAREBANK study is to establish definitive relationships with human cardiac samples and clinical phenotypes in patients undergoing cardiac procedures. Specifically, the investigators aim at comparing atrial phenotypes from atrial fibrillation patients and controls. The work consists of three broad categories: A) role of atrial cardiomyopathy in atrial fibrillation; B) genetic defects predisposing to atrial fibrillation; and C) the role of inflammation in atrial fibrillation.

Detailed description

The investigators aim to A) compare atrial cardiomyopathy findings from the tissue samples to clinical phenotype and adverse events B) study the association of genetic defects predisposing to atrial fibrillation with atrial cardiomyopathy findings in the tissue samples C) assess the role of inflammation in atrial fibrillation by comparing circulating cytokine profiles, purinergic signaling and atrial cardiomyopathy findings in tissue samples.

Interventions

PROCEDURECardiac surgery

Open heart surgery

Sponsors

Brigham and Women's Hospital
CollaboratorOTHER
University of Turku
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

* Any open-heart cardiac surgery * Written informed consent * All-comers design

Exclusion criteria

* No informed consent

Design outcomes

Primary

MeasureTime frameDescription
Atrial fibrillationpostoperatively until 5 years follow-upOccurrence of atrial fibrillation

Secondary

MeasureTime frameDescription
Myocardial infarctionpostoperatively until 5 years follow-upOccurrence of Myocardial infarction
Transient ischemic attackpostoperatively until 5 years follow-upOccurrence of Transient ischemic attack
Strokepostoperatively until 5 years follow-upOccurrence of stroke
Target vessel revascularizationpostoperatively until 5 years follow-upOccurrence of Target vessel revascularization
All-cause Mortalitypostoperatively until 5 years follow-upAll-cause Mortality
Post-pericardiotomy syndromepostoperatively until 1 years follow-upOccurrence of Post-pericardiotomy syndrome

Countries

Finland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 20, 2026