Clinical trial
Signs and Symptoms Associated With Molecular Defects in Genetically Inherited…
NCT00027196 · National Heart, Lung, and Blood Institute (NHLBI), NIH · Completed
Key facts
| NCT number | NCT00027196 |
|---|---|
| Title | Signs and Symptoms Associated With Molecular Defects in Genetically Inherited Heart Disease |
| Official title | Clinical Correlates of Molecular Defects in Familial Cardiomyopathy |
| Lead sponsor | National Heart, Lung, and Blood Institute (NHLBI), NIH |
| Status | Completed |
| Study type | Observational |
| Conditions | Congenital Heart Defect |
| Enrollment | 9,999,999 |
| Start date | Apr 1, 1998 |
| Completion | Apr 1, 2003 |
| First posted | Nov 28, 2001 |
| 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.
About ClinicalTrials.gov studies
ClinicalTrials.gov is the U.S. National Library of Medicine's registry of clinical studies conducted around the world. Contact and investigator details are not shown here.
Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: