CompletedNCT00510302

Melanoma Risk-Reduction Among Patients and Family Members

Studying Familial melanoma

Last synced from ClinicalTrials.gov April 1, 2026

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Key facts

Sponsor: M.D. Anderson Cancer Center
Principal Investigator: Susan Peterson, PhD
M.D. Anderson Cancer Center
Intervention: Questionnaire(behavioral)
Enrollment: 170 target
Eligibility: 18 years · All sexes
Timeline: 2002 – 2020

Study locations (1)

University of Texas MD Anderson Cancer Center, Houston, Texas, United States

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT00510302 on ClinicalTrials.gov

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