DZHK Translational Registry for Cardiomyopathies
- Conditions
- E85I40I42AmyloidosisAcute myocarditisCardiomyopathy
- Registration Number
- DRKS00008017
- Lead Sponsor
- niversitätsklinikum Heidelberg
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 2307
Hereditary and inflammatory dilated cardiomyopathy (DCM)
-Left ventricular dilatation (left ventricular end-diastolic diameter >117%)
-Left ventricular systolic dysfunction
-Hypertrophic cardiomyopathy (HCM)
-Left ventricular non-compaction (LVNC)
-Arrhythmogenic right ventricular cardiomyopathy (ARVC)
-Amyloidosis
-Myocarditis
- <18 years, >80 years
-Other cardiac diseases:
-Severe arterial hypertension
-Primary pulmonary artery hypertension
-Chronic advanced non-cardiac diseases
-History of thorax radiation (life-long)
-Drug and alcohol abuse
-life expectancy <1 year due to non-cardiac diseases
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary endpoint in the TORCH-registry is all-cause death.
- Secondary Outcome Measures
Name Time Method The secondary outcomes are cardiovascular death, adequate ICD shock, survived sudden cardiac death, syncope or documented potentially life-threatening arrhythmia, cardiac transplantation, hospitalization due to the worsening of heart failure, and any non-elective cardiovascular hospitalization.