Clinical trial
Germline Mutations in Patients With Head and Neck Cancer and a Family History of…
NCT00482872 · Vanderbilt University Medical Center, Other · Completed
Key facts
| NCT number | NCT00482872 |
|---|---|
| Title | Germline Mutations in Patients With Head and Neck Cancer and a Family History of Cancer |
| Official title | Familial HNSCC Syndrome and p16 Germline Mutations |
| Lead sponsor | Vanderbilt University Medical Center, Other |
| Collaborators | National Cancer Institute (NCI) NIH |
| Status | Completed |
| Study type | Observational |
| Conditions | Head and Neck Cancer |
| Intervention type | Genetic, Other |
| Interventions | gene expression analysis, mutation analysis, polymerase chain reaction, polymorphism analysis, flow cytometry, laboratory biomarker analysis |
| Enrollment | 400 |
| Start date | Mar 1, 2004 |
| Primary completion | Jul 1, 2012 |
| Completion | Jul 1, 2012 |
| First posted | Jun 5, 2007 |
| Last update posted | Mar 14, 2017 |
| 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: