About this trial
This is an online registry and database of patients with cardiomyopathy and myocarditis, coupled with an observational study of cardiomyopathies.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Adult (age 18 and over),
Males and Females,
Capacity to provide informed consent,
Patients with a confirmed diagnosis of cardiomyopathy or myocarditis,
Disqualifiers
Patients who lack capacity to consent for themselves,
Vulnerable groups (e.g. those under 18, prisoners, those in a dependent relationship, the mentally ill).
who have been informed by their treating physician that their cardiomyopathy is secondary to their coronary artery disease, or
who have undergone previous percutaneous coronary intervention or coronary bypass surgery
Trial population
Eligible adult patients with cardiomyopathy in The Heart Hive registry
Trial design
Cohort
Prospective
Treatments tested in this trial
Research genetic analysis
GeneticGenetic analysis of DNA extracted from saliva. Participants can opt in to receive individual results of research genetic analysis for a predefined panel of clinically actionable cardiomyopathy genes.
Treatment groups
Trial outcomes
Primary outcomes
Number of participants with cardiovascular cause of death
Cardiovascular death
Number of participants with arrhythmic events
(ventricular fibrillation, unstable sustained ventricular tachycardia, appropriate implantable cardioverter-defibrillator delivered shock, and aborted sudden cardiac death
Number of participants with major heart failure events
heart transplantation, left ventricular assist device implantation, unplanned heart failure, hospitalisation
Sponsors and contacts
Click on the lead sponsor to view all of their trials.