Clinical trial
Study of Heritable Connective Tissue Disorders
NCT00001641 · National Human Genome Research Institute (NHGRI), NIH · Completed
Key facts
| NCT number | NCT00001641 |
|---|---|
| Title | Study of Heritable Connective Tissue Disorders |
| Official title | Clinical and Molecular Manifestations of Heritable Connective Tissue Disorders |
| Lead sponsor | National Human Genome Research Institute (NHGRI), NIH |
| Status | Completed |
| Study type | Observational |
| Conditions | Connective Tissue Disease, Dissecting Aneurysm, Ehlers Danlos Syndrome, Marfan Syndrome, Nail Patella Syndrome |
| Enrollment | 900 |
| Start date | Mar 1, 1997 |
| Completion | Jun 1, 2002 |
| First posted | Nov 4, 1999 |
| 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: