TranslatiOnal Registry for CardiomyopatHies (TORCH) - Plus as Part of the German Centre for Cardiovascular Research (DZHK)

Status: Recruiting
Location: See location...
Study Type: Observational
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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 80
Healthy Volunteers: f
View:

• Non-ischemic structural cardiomyopathies

• Age ≥ 18 or ≤ 80 years

• The patient is able to understand the declaration of consent and to sign it dated

• At least one of the following diagnoses depending on the specific TORCH-

⁃ Plus inclusion / exclusion - SOP:

⁃ Dilated Cardiomyopathy (DCM)

• family / genetic

• inflammatory / persistent myocarditis

• idiopathic (after exclusion secondary cause)

• left sided systolic dysfunction (EF ≤ 45%)

⁃ Left ventricular hypertrophy

• sarcomere hypertrophic cardiomoypathia (HCM, HOCM)

• amyloid (AL: light chains, TTR: transthyretin, wild type)

⁃ Left ventricular non-compaction cardiomyopathy (LVNC)

⁃ Arrhythmogenic right ventricular cardiomyopathy (ARVC / D)

Locations
Other Locations
Germany
University Hospital Heidelberg - Clinic of Cardiology, Angiology and Pneumology
RECRUITING
Heidelberg
Contact Information
Primary
Farbod Sedaghat-Hamendani, Dr.
Farbod.Sedaghat-Hamedani@med.uni-heidelberg.de
+496221/56-8676
Backup
Johannes Trebing, Dr.
Johannes.Trebing@med.uni-heidelberg.de
Time Frame
Start Date: 2020-08-18
Estimated Completion Date: 2027-12
Participants
Target number of participants: 2040
Sponsors
Collaborators: Charite University, Berlin, Germany, Deutsches Herzzentrum Muenchen, University Hospital Schleswig-Holstein, University Medicine Greifswald, Goethe University, University Medical Center Goettingen, Universitätsklinikum Hamburg-Eppendorf, University Hospital Munich, University of Mannheim, Medical University of Hannover, Technical University of Munich, Kerckhoff Klinik, German Heart Center, University Medical Center Mainz
Leads: University Hospital Heidelberg

This content was sourced from clinicaltrials.gov