Viewing Study NCT00221832

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Ignite Creation Date: 2025-12-24 @ 9:58 PM
Ignite Modification Date: 2026-03-05 @ 9:20 PM
Study NCT ID: NCT00221832
Status: UNKNOWN
Last Update Posted: 2010-01-13
First Post: 2005-09-14
Is NOT Gene Therapy: True
Has Adverse Events: False
Brief Title: Molecular Genetic Screening and Identification of Congenital Arrhythmogenic Diseases
Sponsor: Heidelberg University
Organization:
Overview Dates Organization Conditions Design Enrollment Locations Outcomes Modules Raw JSON

Conditions & Keywords Data

Conditions:

Conditions

Condition Brief Condition Text View
None Long QT Syndrome View
None Hypertrophic Cardiomyopathy View
None Arrhythmogenic Right Ventricular Dysplasia View
Keywords:

Keywords

Keyword Brief Keyword Text View
None Long QT Syndrome View
None Hypertrophic cardiomyopathy View
None arrhythmogenic right ventricular dysplasia View
None Short QT Syndrome View
None Brugada Syndrome View