Status:
COMPLETED
Pilot Study of Infrared Imaging of Cutaneous Melanoma
Lead Sponsor:
University of Virginia
Conditions:
Melanoma
Eligibility:
All Genders
18+ years
Brief Summary
Design: this is a pilot study of infrared imaging of cutaneous lesions in patients and volunteers with and without clinically detectable melanoma, and with one or more palpable cutaneous lesions eligi...
Eligibility Criteria
Inclusion
- Patients or volunteers with or without a history of melanoma.
- One or more palpable skin or subcutaneous lesions for which at least one of the following is true:
- A tissue diagnosis has been made for the lesion(s) in question, by prior cytologic or histologic evaluation (Category A1).
- A tissue diagnosis will be obtained for the lesion(s) in question by cytologic or histologic evaluation (Category A2).
- A tissue diagnosis is not available, but a clinical diagnosis of melanoma or benign lesion is available with a high degree of confidence. Examples are hemangiomas, skin tags, seborrheic keratoses, dermatofibromas, lipomas, or growing pigmented skin lesions that are comparable to other cutaneous metastases of melanoma in the same patient (Category B).
- All patients must have the ability and willingness to give informed consent and must be age 18 years or older at the time of study entry.
Exclusion
- Known or suspected allergy to the adhesive skin markers or water-soluble ink used for the labeling of lesions.
- Very fragile skin that may be susceptible to injury from adhesive markers.
- Patients in whom there is a medical contraindication or potential problem in complying with the requirements of the protocol, in the opinion of the investigator.
Key Trial Info
Start Date :
March 1 2008
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
Estimated Enrollment :
74 Patients enrolled
Trial Details
Trial ID
NCT00937690
Start Date
March 1 2008
Last Update
December 23 2014
Active Locations (1)
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1
University of Virginia
Charlottesville, Virginia, United States, 22908