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NCT03683836 Clinical Trial

Minor Troponin Elevations in Patients With Atrial Fibrillation

Atrial Fibrillation Clinical Trial

— Tropo-AF  

Official title:
Etiology of Minor Troponin Elevations in Patients With Atrial Fibrillation Visiting Emergency Department

Clinical Trial Details — Status: Active, not recruiting

Administrative data
NCT number NCT03683836
Other study ID # T125/2016
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date June 1, 2016
Est. completion date October 30, 2023

Study information
Verified date June 2022
Source University of Turku
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study aims at identifying the etiology of troponin-T elevations in patients with atrial fibrillation visiting the emergency department.

Description:

The aim of this study is to identify the factors associated with minor cardiac troponin-T elevations in patients presenting in emergency department (ED) with atrial fibrillation (AF) diagnosis , and the possible implications it has on the patients prognosis. Data on 3394 patients from the Turku university hospital catchment area with diagnosis of AF on admission to ED and minor troponin-T elevation were analyzed. Patients were classified into three groups according to the troponin-T value: troponin <15ng/l, 15-50ng/l and 51-100ng/l. Individual patient records were reviewed.

Recruitment information / eligibility
Status Active, not recruiting
Enrollment 3394
Est. completion date October 30, 2023
Est. primary completion date October 30, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - two troponin T tests within 72 hours of ED admission - Prior diagnosis of AF or AF at admission Exclusion Criteria: - Age < 18 years

Study Design

Related Conditions & MeSH terms

Intervention

Diagnostic Test:
• No intervention
No intervention

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
University of Turku

Outcome
Type Measure Description Time frame Safety issue
Primary All-cause mortality, myocardial infarction, ischemic stroke Major adverse cardiac or cerebrovascular event within one year 12 months
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