Clinical trial
Signs and Symptoms of Genetic Abnormalities Linked to Inherited Heart Disease
NCT00001881 · National Heart, Lung, and Blood Institute (NHLBI), NIH · Completed
Key facts
| NCT number | NCT00001881 |
|---|---|
| Title | Signs and Symptoms of Genetic Abnormalities Linked to Inherited Heart Disease |
| Official title | Clinical Manifestations of Mutations in Genes Linked to Familial Cardiomyopathy |
| Lead sponsor | National Heart, Lung, and Blood Institute (NHLBI), NIH |
| Status | Completed |
| Study type | Observational |
| Conditions | Cardiomyopathy, Hypertrophic, Familial |
| Enrollment | 9,999 |
| Start date | Mar 1, 1999 |
| Completion | Apr 1, 2001 |
| First posted | Dec 10, 2002 |
| Last update posted | Mar 4, 2008 |
| Countries | United States |
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: