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Storage and Research Use of Human Bio-specimens From Melanoma Patients and Clinical Testing for Assignment of Treatment

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Vanderbilt University Medical Center

Status

Enrolling

Conditions

Melanoma

Treatments

Other: Tissue and blood collection

Study type

Observational

Funder types

Other

Identifiers

NCT01205815
VICC MEL 09109

Details and patient eligibility

About

The purpose of this research is to identify biological characteristics occurring in the initiation and progression of melanoma.

Enrollment

3,000 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion criteria

  • Pathologically-proven diagnosis of melanoma.
  • Patient must have a test or procedure that has the potential to provide left-over tissue that can be banked for future research purposes OR the patient has already had a diagnostic or therapeutic procedure but who has not yet been approached to participate is also eligible.

Exclusion criteria

  • Any patient with significant contraindications to venipuncture (e.g., severe anemia) will be excluded from blood collection procedures. However, if the patient provides consent and a paraffin-embedded block or 10-15 unstained slides of their tissue diagnosis, they will not be excluded from this protocol.
  • Any patient unable or unwilling to provide consent.

Trial contacts and locations

1

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Central trial contact

Vanderbilt-Ingram Service for Timely Access

Data sourced from clinicaltrials.gov

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