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NCT02668614 Clinical Trial

Early Detection of Skin Cancer With Sensor Technology

Carcinoma, Basal Cell Clinical Trial

Official title:
Early Detection of Skin Cancer Using Millimetre-Wave Waveguide Reflectometers

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02668614
Other study ID # HSREB 107218
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 2016
Est. completion date February 2018

Study information
Verified date November 2018
Source Lawson Health Research Institute
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Skin cancer represents a large problem in today's healthcare setting. The majority of cancer diagnoses are attributed to malignant skin diseases including its major types: basal cell carcinoma, squamous cell carcinoma and melanoma. Early diagnoses is critical given early detection of malignant lesions largely increases chances of successful treatment. The current gold standard of diagnosis is histopathological examination of biopsied skin. Biopsies are not only invasive and expensive, they have variable positive predictive value, meaning they may often be preformed unnecessarily. As such, the investigators have developed a skin scanner, which is less bulky and expensive than existing similar technologies, as a tool to evaluate skin lesions prior to determining the need for a biopsy. Their objective is to obtain information in order to validate this skin scanner in the context of its ability to accurately identify basal cell carcinoma skin lesions.

Recruitment information / eligibility
Status Completed
Enrollment 60
Est. completion date February 2018
Est. primary completion date February 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patient requiring skin biopsy for suspected basal cell carcinoma skin lesion

- 18 years of age or older

Exclusion Criteria:

-Poor english fluency, Pregnancy

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• WR-22 model microwave sensor

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Lawson Health Research Institute

Outcome
Type Measure Description Time frame Safety issue
Primary Positive predictive value Immediately pre-biopsy
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