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Studying Heart Muscle Weakness Caused by Irregular Heartbeat

Collects existing data from adults suspected of having arrhythmia-induced cardiomyopathy at Basel.

Plain-language title generated from the registry record
Registry title: Characterization of Arrhythmia-induced Cardiomyopathy

Key facts

Where
Basel, SwitzerlandSee the site

Where in Switzerland

  • University Hospital Basel, Department of CardiologyBasel, SwitzerlandTaking people

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  4. What happens if I want to stop?
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Trial details

Who runs it
University Hospital, Basel, Switzerland
Trial code
NCT05662293
Record updated
4 March 2025
Original description
The goal of the this observational study is to gather clinically available data on patients presenting with a suspicion for arrhythmia-induced cardiomyopathy (AiCM) at the University Hospital Basel.Read full original descriptionShow less

Arrhythmia-induced Cardiomyopathy - a Prospective Observational Cohort Study

The goal of the this observational study is to gather clinically available data on patients presenting with a suspicion for arrhythmia-induced cardiomyopathy (AiCM) at the University Hospital Basel.

Inclusion: Diagnostic or suspicion of AiCM as presence of specified keyword in patient's file or as screened by colleagues of the internal medicine or cardiology clinics; Signed study consent; Patients with a reduced left-ventricular ejection fraction (LVEF ≤50%) or a reduction of 15% in the ejection fraction (EF) between two echocardiographies and a concomitant diagnosis of any arrhythmia likely to lead to AiCM within one year before or after diagnosis of the reduced LVEF from 2010-2021.

Exclusion: Temporary exclusion criteria: Acute health condition such as myocardial infarction, patients presenting with a major trauma, a sepsis, patients shortly after cardiac surgery, and patients in shock (>100 bpm, <90 systolic BP, evidence of organ dysfunction); Life expectancy <1 year (palliative, terminal cancer); Retrospective part; Patients with life expectancy <1 year (palliative, terminal cancer); Acute event clearly leading to an acutely reduced LVEF (massive type I myocardial infarction, cardiogenic shock from a coronary or myocardial etiology, septic shock leading to toxic myopathy, hypovolemic shock with reduced EF, cardiac arrest and/or need for resuscitation); Age <18 years old; Age < 18 years old; Patient's active refusal of the general consent of the University Hospital Basel; Patient's active refusal of the general consent of the University Hospital Basel.

Prospective part.

ClinicalTrials.gov NCT05662293