Characterization of Arrhythmia-induced Cardiomyopathy
Launched by UNIVERSITY HOSPITAL, BASEL, SWITZERLAND · Dec 14, 2022
Trial Information
Current as of June 26, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is studying a condition called arrhythmia-induced cardiomyopathy (AiCM), which is a type of heart problem that can happen when the heart beats irregularly. The goal of the study is to collect information from patients who may have this condition at the University Hospital Basel. Researchers want to understand how AiCM affects people and gather data that can help improve care for patients with this heart issue.
To participate in the trial, individuals should be between the ages of 65 and 74 and have a diagnosis or suspicion of AiCM. They must also agree to take part by signing a consent form. However, people who are younger than 18, have certain serious health conditions, or who do not wish to participate cannot join the study. Participants can expect to share their medical information and undergo assessments related to their heart health. It's important to note that this study is observational, meaning researchers will be collecting existing data rather than providing treatment.
Gender
ALL
Eligibility criteria
- • Prospective part
- Inclusion Criteria:
- • 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
- Exclusion Criteria:
- • Patient's active refusal of the general consent of the University Hospital Basel
- • Age \<18 years old
- • 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
- Inclusion Criteria:
- • 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 Criteria:
- • Age \< 18 years old
- • Patient's active refusal of the general consent of the University Hospital Basel
- • 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).
- • Patients with life expectancy \<1 year (palliative, terminal cancer)
About University Hospital, Basel, Switzerland
The University Hospital Basel, Switzerland, is a leading academic medical center renowned for its commitment to cutting-edge research and innovative patient care. As a prominent clinical trial sponsor, the hospital leverages its extensive expertise and state-of-the-art facilities to advance medical knowledge and therapeutic options across various disciplines. With a collaborative approach that integrates clinical practice and scientific inquiry, the University Hospital Basel fosters an environment conducive to rigorous clinical trials, ensuring the highest standards of safety and efficacy. Its strategic focus on patient-centered research aims to translate scientific discoveries into tangible health solutions, benefiting both local and global communities.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Basel, , Switzerland
Patients applied
Trial Officials
Patrick Badertscher, MD
Principal Investigator
University Hospital Basel, Department of Cardiology
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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