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

No results posted yet for this study

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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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04265040 on ClinicalTrials.gov