DZHK TORCH-Plus is a Registry for Patients With Cardiomyopathies and Serves as Source for Cardiovascular Research Studies
NCT04265040 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 2040
Last updated 2023-11-30
Summary
The DZHK TranslatiOnal Registry for CardiomyopatHies (DZHK TORCH) represents a unique resource of clinical data and high quality biological samples to enable innovative clinical and molecular studies on cardiomyopathies (CMP). As a multi-center German cardiomyopathy registry, TORCH has been prospectively admitting patients since December 2014. 2,300 patients were recruited as planned. Taken together, patient data showed that the prevalence of these diseases is much higher in men than in women, atrial fibrillation is common in all forms of CMPs as well as rare forms of disease indicate a higher risk and higher morbidity.
This DZHK TORCH register is now to be expanded with a second phase (DZHK TORCH-Plus). The second phase DZHK TORCH-Plus consists of 4 main modules: 1. "Clinical phenotyping, follow-up \& biosampling" 2. "Genomics", 3. "Inflammation" and 4. "Biomarker". The central aims are 1) to significantly increase the number of probands (n = 4340) in order to better address the different types of CMPs, especially patients with rare CMP forms such as LVNC and ARVC or with probably molecularly explainable cardiomyopathies (familial DCM), 2) to prolong the longitudinal with a further follow-up to achieve sufficient events and thereby derive clinical recommendations for risk assessment, 3) to increase the number of probands with state-of-the-art phenotyping, 4) to pinpoint the effect of myocardial inflammation, fibrosis, gender and to determine or predict genotypes based for outcome, 5) to validate novel biomarkers developed in other DZHK studies, and 6) to foster active cooperation with international CMP registries and partners from industry.
Conditions
- Non-ischemic Cardiomyopathy
- DCM - Dilated Cardiomyopathy
- HCM - Hypertrophic Cardiomyopathy
- HOCM - Hypertrophic Obstructive Cardiomyopathy
- Arrhythmogenic Right Ventricular Cardiomyopathy
- Left Ventricular Noncompaction Cardiomyopathy
- Amyloidosis
- Inflammatory Cardiomyopathy
Sponsors & Collaborators
-
University Medicine Greifswald
collaborator OTHER -
Charite University, Berlin, Germany
collaborator OTHER -
German Heart Center
collaborator OTHER -
University of Mannheim
collaborator OTHER -
University Hospital Schleswig-Holstein
collaborator OTHER -
Medical University of Hannover
collaborator OTHER -
Goethe University
collaborator OTHER -
Universitätsklinikum Hamburg-Eppendorf
collaborator OTHER -
University Medical Center Mainz
collaborator OTHER -
University Medical Center Goettingen
collaborator OTHER -
Deutsches Herzzentrum Muenchen
collaborator OTHER -
Technical University of Munich
collaborator OTHER -
University Hospital Munich
collaborator OTHER -
Kerckhoff Klinik
collaborator OTHER -
University Hospital Heidelberg
lead OTHER
Eligibility
- Min Age
- 18 Years
- Max Age
- 80 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2020-08-18
- Primary Completion
- 2027-12-31
- Completion
- 2027-12-31
Countries
- Germany
Study Locations
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