Clinical trial
Identifying Gene Mutations in Patients With Melanoma and in Families With a…
NCT00450593 · Leeds Cancer Centre at St. James's University Hospital, Other · Unknown status
Key facts
| NCT number | NCT00450593 |
|---|---|
| Title | Identifying Gene Mutations in Patients With Melanoma and in Families With a History of Hereditary Melanoma |
| Official title | Studies of Familial Melanoma |
| Lead sponsor | Leeds Cancer Centre at St. James's University Hospital, Other |
| Status | Unknown status |
| Study type | Observational |
| Conditions | Hereditary Multiple Melanoma, Melanoma (Skin) |
| Intervention type | Genetic, Other, Procedure |
| Interventions | gene expression analysis, microarray analysis, molecular genetic technique, mutation analysis, laboratory biomarker analysis, mutation carrier screening, study of high risk factors |
| Enrollment | 5,000 |
| Start date | Jan 1, 1989 |
| Primary completion | Dec 1, 2020 |
| First posted | Mar 22, 2007 |
| Last update posted | Aug 12, 2013 |
| Countries | United Kingdom |
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: