Clinical trial
Studies of Heritable Disorders of Connective Tissue
NCT00270686 · National Institute on Aging (NIA), NIH · Completed
Key facts
| NCT number | NCT00270686 |
|---|---|
| Title | Studies of Heritable Disorders of Connective Tissue |
| Official title | Clinical and Molecular Manifestations of Heritable Disorders of Connective Tissue |
| Lead sponsor | National Institute on Aging (NIA), NIH |
| Status | Completed |
| Study type | Observational |
| Conditions | Ehlers-Danlos Syndrome, Stickler Syndrome, Marfan Syndrome |
| Enrollment | 929 |
| Start date | Jan 21, 2003 |
| Completion | Jan 2, 2015 |
| First posted | Dec 28, 2005 |
| Last update posted | Apr 5, 2018 |
| 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: