Clinical trial
Genetic Study to Identify Gene Mutations in Participants Previously Enrolled in…
NCT00075348 · National Institutes of Health Clinical Center (CC), NIH · Completed
Key facts
| NCT number | NCT00075348 |
|---|---|
| Title | Genetic Study to Identify Gene Mutations in Participants Previously Enrolled in Clinical Trial NCI-99-C-0053 Who Have Von Hippel-Lindau Syndrome or Are at Risk for Von Hippel-Lindau Syndrome |
| Official title | Genetic Mutation Analysis In A VHL Population |
| Lead sponsor | National Institutes of Health Clinical Center (CC), NIH |
| Collaborators | National Cancer Institute (NCI) NIH |
| Status | Completed |
| Study type | Observational |
| Conditions | Kidney Cancer, Von Hippel-lindau Syndrome |
| Intervention type | Genetic |
| Interventions | mutation analysis |
| Enrollment | 260 |
| Start date | Dec 1, 2003 |
| Primary completion | Dec 1, 2008 |
| Completion | Dec 1, 2008 |
| First posted | Jan 12, 2004 |
| Last update posted | Mar 15, 2012 |
| 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: