Basal Cell Carcinoma Clinical Trial
Official title:
An Observational Study to Determine the Clinical Cure Rate of Therapeutic up Front Shave Removal of Basal Cell Carcinoma of the Skin With Long Term Follow up to Evaluate Recurrence
NCT number | NCT02296970 |
Other study ID # | PRO14020682 |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | December 2014 |
Est. completion date | December 31, 2018 |
Verified date | April 2019 |
Source | University of Pittsburgh |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
Determine the effectiveness of a deep shave removal as a definitive treatment for basal cell carcinoma (BCC) without the need for a follow up surgical procedure.
Status | Completed |
Enrollment | 78 |
Est. completion date | December 31, 2018 |
Est. primary completion date | June 2016 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Patients 18 years or older that are determined by an investigator to have a lesion that is highly likely to be a BCC, less than or equal to 1.0cm in largest diameter, based on clinical examination located in the trunk or extremities, proximal to the wrist and ankles - Subject is able to give informed consent - Subject is able to commit to 6 month follow up visit Exclusion Criteria: - BCC > 1cm in diameter on any one axis. - Immunosuppressed patients - Subjects with neutropenia - Organ transplant patients - Subjects with a life expectancy less than year - Patients taking immunosuppressive medications, including prednisone at a dose of 10mg or greater with an expected duration greater than 4 weeks, azathioprine, mycophenolate mofetil, cyclosporine, oral Tacrolimus, any Tumor Necrosis Factor (TNF)-alpha inhibitor, ustekinumab, rituximab, or any other medication in the judgement of the investigator could results in clinically meaningful immunosuppression of the subject - Basal cell carcinomas that have infiltrative or morpheaform characteristics based on clinical examination - Subjects unable to provide informed consent - Subjects unable to commit to 6 month follow up |
Country | Name | City | State |
---|---|---|---|
United States | Shadyside Place | Pittsburgh | Pennsylvania |
Lead Sponsor | Collaborator |
---|---|
University of Pittsburgh |
United States,
Ahnlide I, Bjellerup M. Accuracy of clinical skin tumour diagnosis in a dermatological setting. Acta Derm Venereol. 2013 May;93(3):305-8. doi: 10.2340/00015555-1560. — View Citation
Ek EW, Giorlando F, Su SY, Dieu T. Clinical diagnosis of skin tumours: how good are we? ANZ J Surg. 2005 Jun;75(6):415-20. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Measurement of clinical cure rate of deep shave removal in the treatment of BCC | 6 months | ||
Secondary | Percentage of deep shave removal BCC with clear margins | 6 months |
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