ACTRN12616000272493
Active, not recruiting
未知
A longitudinal, observational study investigating pigmentation genotypes and phenotypic correlations with dermoscopic naevus types and distribution in two participant groups; advanced stage melanoma patients undergoing targeted and/or immunotherapies, and a 'high risk' melanoma patient group.
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Melanoma
- Sponsor
- The University of Queensland
- Enrollment
- 170
- Status
- Active, not recruiting
- Last Updated
- 6 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Cohort 1: melanoma patients with stage III and IV enrolled for treatment with targeted therapies and/or immunotherapies at the Cancer Services (PA Hospital). Baseline visit must be within 6 weeks of beginning melanoma treatment.
- •Cohort 2: participants considered high risk for melanoma under at least one of the following three subcategories;
- •a)Personal history of melanoma (stage I\-IV, not in situ)
- •b)First degree family history of melanoma (stage I\-IV, not in situ)
- •c)Atypical mole syndrome, defined as grater then 100 naevi, 6 (or more) atypical naevi (confirmed using dermoscopy), AND at least 1 naevus 8 mm (or greater) in dimension.
Exclusion Criteria
- •All participants must be able to give informed consent.
- •All participants are asked to commit to 4 visits to the PA Hospital to participate in the trial over a 12 month period (months 0, 4, 8 and 12\), as long as they are able to (Participants can withdraw from the study at any time for any reason).
- •Participants in cohort 2 must not be currently undergoing any treatment for melanoma.
Outcomes
Primary Outcomes
Not specified
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