Clinical trial
Diagnostic and Screening Study of Genetic Disorders
NCT00006057 · National Center for Research Resources (NCRR), NIH · Completed
Key facts
| NCT number | NCT00006057 |
|---|---|
| Title | Diagnostic and Screening Study of Genetic Disorders |
| Lead sponsor | National Center for Research Resources (NCRR), NIH |
| Collaborators | Icahn School of Medicine at Mount Sinai |
| Status | Completed |
| Study type | Observational |
| Conditions | Tay-Sachs Disease, Porphyria, Erythropoietic, Leukodystrophy, Globoid Cell, Metabolism, Inborn Errors |
| Enrollment | 50 |
| Start date | Dec 1, 1999 |
| First posted | Jul 6, 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: