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Storing blood and tumor samples from people with skin cancer for research

Collects and keeps blood and tumor samples from people with melanoma and healthy volunteers.

Key facts

Who runs it
Ohio State University Comprehensive Cancer Center
Where
Columbus, United StatesSee the site
Trial code
Registry title
A Storage Facility for Tissues Obtained From Patients With Malignant Melanoma
Status
Recruiting
People taking part
1,000 people, planned
Started
7 May 2013
Expected to end
31 Oct 2027
Type of study
Observational
Treatments tested
  • Biospecimen Collection
Record updated
17 February 2026

Who can take part

AI summary

From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.

The trial is looking for people with malignant melanoma, or a past history of melanoma, and for healthy donors. Blood and tumor samples are collected and stored for future research.

Sex
All sexes can join.
Disease stage
Any stage of malignant melanoma.

Main reasons for not taking part

  • Incarcerated individuals cannot join.

The registry criteria, word for word

Show all 5 criteriaShow less

Who can take part

  • Patient with malignant melanoma or personal history of melanoma
  • Normal donors
  • Informed consent can be obtained
  • Patients with any stage of malignant melanoma

Who cannot take part

  • Incarcerated individuals will be excluded from this protocol

Where in United States

  • Ohio State University Comprehensive Cancer CenterColumbus, United StatesContact: William E. Carson, MDTaking people

About the trial

What the trial wants to find out

This study collects and stores blood and tumor samples from patients with malignant melanoma and healthy individuals. The purpose of this study is to gain a better understanding of the causes of melanoma and how melanoma tumors behave. Storing blood and tumor samples for future research may lead to new discoveries that may ultimately help with diagnosing or treating this disease.

The group in the trial

  • Ancillary-correlative (biospecimen collection)

    Patients undergo collection of blood samples at the time of the initial diagnostic work-up, and possibly prior to the initiation of surgery, chemotherapy, immunotherapy, or radiation therapy, at tumor progression or recurrence, and annually during routine follow-up (no more than 4 blood draws per year). Patients may also undergo collection of tissue sample during standard of care surgical or radiologic procedures. Healthy individuals undergo collection of blood samples up to 4 times over 1 year.

    Treatment: Biospecimen Collection

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Data and sources

Registry record
Listed on ClinicalTrials.gov.
Official title
Analysis of the Tumor Microenvironment and Immune Response in Malignant Melanoma
Plain-language title
Storing blood and tumor samples from people with skin cancer for researchGenerated from the registry record. The registry title is the official one.
AI summary
From the trial's eligibility criteria. Read by machine on 12 November 2026.
Record updated
17 February 2026