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Risk Stratification in Children and Adolescents With Primary Cardiomyopathy (RIKADA)

G

German Heart Institute

Status

Unknown

Conditions

Primary Cardiomyopathy
Arrhythmogenic Right Ventricular Cardiomyopathy
Restrictive Cardiomyopathy
Hypertrophic Cardiomyopathy
Dilated Cardiomyopathy
Left Ventricular Noncompaction

Study type

Observational

Funder types

Other

Identifiers

NCT03572569
A30127
81Z3100331 (Other Grant/Funding Number)

Details and patient eligibility

About

RIKADA is a prospective study performing systematic family screening including clinical and genetic testing in pediatric patients with primary cardiomyopathy and their first-degree relatives with the aim to facilitate risk stratification.

Full description

RIKADA is a long-term prospective study performing in-depth phenotype and genotype characterization in children and adolescents with primary cardiomyopathy and their first-degree family members. Family screening contains complete cardiac work-up with medical history, physical examination, 12-lead-/Holter-electrocardiogram, cardiopulmonary exercise testing, echocardiography, cardiovascular magnetic resonance (CMR) and laboratory including genetic testing. The aim is to facilitate early identification of at-risk individuals and contribute to patient-specific follow-up and therapy regimes preventing progressive heart failure and arrhythmia in pediatric CMP.

Enrollment

200 estimated patients

Sex

All

Ages

Under 18 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Index patients:

    • Age ≤18 years
    • written informed consent of parents/legal guardians
    • diagnosis of primary cardiomypathy:
    • DCM: left ventricular (LV) systolic dysfunction and dilatation greater than two standard deviations (SD) above the mean of a normal population
    • HCM: LV hypertrophy and septal wall thickness above two SD
    • RCM: diastolic dysfunction and concordant atrial enlargement
    • LVNC: separation of the myocardium into a compacted (C) and a non- compacted (NC) layer with an NC/C ratio >2 in echocardiography and/or >2.3 in CMR
    • ARVC: according to the revised Task Force Criteria
  2. First-degree family members (parents and siblings):

    • Age ≥3 years
    • written informed consent of parents/legal guardians and siblings ≥18 years

Exclusion criteria

  • unwillingness to give consent
  • myocardial inflammation / myocarditis
  • systemic disease with cardiac involvement (secondary cardiomyopathy)
  • structural congenital heart disease

Trial design

200 participants in 2 patient groups

Index patients
Description:
Patients ≤18 years with primary cardiomyopathy
First-degree family members
Description:
Parents and siblings of index patients

Trial contacts and locations

2

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Central trial contact

Nadya Al-Wakeel-Marquard, MD; Sabine Klaassen, MD

Data sourced from clinicaltrials.gov

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