# Identifying Gene Mutations in Patients With Melanoma and in Families With a History of Hereditary Melanoma

> **NCT00450593** · — · UNKNOWN · sponsor: **Leeds Cancer Centre at St. James's University Hospital** · enrollment: 5000 (estimated)

## Conditions studied

- Hereditary Multiple Melanoma
- Melanoma (Skin)

## Interventions

- **GENETIC:** gene expression analysis
- **GENETIC:** microarray analysis
- **GENETIC:** molecular genetic technique
- **GENETIC:** mutation analysis
- **OTHER:** laboratory biomarker analysis
- **PROCEDURE:** mutation carrier screening
- **PROCEDURE:** study of high risk factors

## Key facts

- **NCT ID:** NCT00450593
- **Lead sponsor:** Leeds Cancer Centre at St. James's University Hospital
- **Sponsor class:** OTHER
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** UNKNOWN
- **Start date:** 1989-01
- **Primary completion:** 2020-12
- **Final completion:** —
- **Target enrollment:** 5000 (ESTIMATED)
- **Last updated:** 2013-08-12


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT00450593

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT00450593, "Identifying Gene Mutations in Patients With Melanoma and in Families With a History of Hereditary Melanoma". Retrieved via AI Analytics 2026-06-25 from https://api.ai-analytics.org/clinical/NCT00450593. Licensed CC0.

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