Clinical trial
Molecular Genetic Screening and Identification of Congenital Arrhythmogenic…
NCT00221832 · Heidelberg University, Other · Unknown status
Key facts
| NCT number | NCT00221832 |
|---|---|
| Title | Molecular Genetic Screening and Identification of Congenital Arrhythmogenic Diseases |
| Official title | Molecular Genetic Screening and Identification of Congenital Arrhythmogenic Diseases |
| Lead sponsor | Heidelberg University, Other |
| Status | Unknown status |
| Study type | Observational |
| Conditions | Long QT Syndrome, Hypertrophic Cardiomyopathy, Arrhythmogenic Right Ventricular Dysplasia |
| Enrollment | 300 |
| Start date | Oct 1, 2003 |
| Completion | Dec 1, 2011 |
| First posted | Sep 22, 2005 |
| Last update posted | Jan 13, 2010 |
| Countries | Germany |
At a glance
- 1–9 Study sites
- No Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: