Clinical trial
Genes Causing Ebstein's Anomaly
NCT00497705 · National Heart, Lung, and Blood Institute (NHLBI), NIH · Completed
Key facts
| NCT number | NCT00497705 |
|---|---|
| Title | Genes Causing Ebstein's Anomaly |
| Official title | Genes Causing Congenital Ebstein's Anomaly |
| Lead sponsor | National Heart, Lung, and Blood Institute (NHLBI), NIH |
| Status | Completed |
| Study type | Observational |
| Conditions | Heart Septal Defects, Ventricle, Heart Defects, Congenital, Double Outlet Right Ventricle, Truncus Arteriosus, Persistent |
| Start date | Jul 3, 2007 |
| Primary completion | Jul 7, 2009 |
| First posted | Jul 9, 2007 |
| Last update posted | Jul 2, 2017 |
| Countries | Belarus, Ukraine, 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: