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Genetic Basis of Melanocytic Nevi

Recruiting
Conditions
Melanocytic Nevi
Registration Number
NCT03054584
Lead Sponsor
University of California, Davis
Brief Summary

The objective of this protocol is to further elucidate the genetic mutations that drive melanocytic nevi (benign melanocytic neoplasms, moles). This will be performed by whole genome, whole exome, or targeted sequencing of de-identified specimens.

Herein, the investigators plan to isolate DNA from de-identified skin biopsy specimens and blood samples:

1. From melanocytic nevi collected by skin biopsy (a shave or punch biopsy). A part of the tissue will be submitted for routine diagnostic dermatopathology and investigational histomorphologic and immunohistochemical analysis.

2. From corresponding normal tissue (blood). DNA isolated from blood will be used as a normal control when analyzing sequencing data to identify somatic mutations in lesional tissue.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
50
Inclusion Criteria

Not provided

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Exclusion Criteria

Not provided

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Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Genome Wide Mutation AnalysisFeb 2017 - December 2018

Will be performing genome wide mutation analysis to quantify the number of mutations.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

University of California-Davis, Department of Dermatology

🇺🇸

Sacramento, California, United States

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