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
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Contact the study team: see the registry record → Contacts and Locations
Print a page for my doctorData 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