Clinical trial
Genetic Study of the FBN1 Gene and Fibrillin-1 Abnormalities in Choctaw Native…
NCT00006393 · National Center for Research Resources (NCRR), NIH · Unknown status
Key facts
| NCT number | NCT00006393 |
|---|---|
| Title | Genetic Study of the FBN1 Gene and Fibrillin-1 Abnormalities in Choctaw Native Americans and Other Patients With Systemic Sclerosis |
| Official title | Genetic Study of the FBN1 Gene and Fibrillin-1 Abnormalities in Choctaw Native Americans and Other Patients With Systemic Sclerosis |
| Lead sponsor | National Center for Research Resources (NCRR), NIH |
| Collaborators | University of Texas |
| Status | Unknown status |
| Study type | Observational |
| Conditions | Systemic Sclerosis |
| Enrollment | 80 |
| Start date | Jul 1, 1998 |
| First posted | Oct 5, 2000 |
| Last update posted | Jun 24, 2005 |
| 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: