Melanoma Clinical Trial
5-year Study to Track Clinical Application of DecisionDx-Melanoma Gene Expression Profile Assay Results
Summary
The INTEGRATE Registry Study follows patients with cutaneous melanoma who have had the DecisionDx-Melanoma gene expression assay performed. Data will be collected through review of medical records from clinical visits with physician.
The purpose is to document the clinical application of results obtained from the DecisionDx- Melanoma multi-gene assay and to track outcomes of patients for whom DecisionDx-Melanoma testing has been completed. Additionally the study will assess the health economic impact of DecisionDx-Melanoma testing as it relates to the Melanoma population.
Eligibility Criteria
Inclusion Criteria:
Patients diagnosed with melanoma and determined, by their physician, to be appropriate for DecisionDx-Melanoma testing and who have successful results available to the investigator are eligible for registration
Patients enrolled should be reasonably able to follow-up with the enrolling physician at regular intervals for assessment of outcome data.
16 Years and older
Exclusion Criteria:
Less than 16 Years of age
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There are 3 Locations for this study
Atlanta Georgia, 30342, United States
Louisville Kentucky, 40202, United States
Saint Louis Missouri, 63103, United States
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