Expired Study
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Louisville, Kentucky 40217


Purpose:

This study compares HP802-247 versus an antibiotic ointment for healing the wound after Mohs surgery.


Criteria:

Inclusion Criteria: - Provide informed consent. - Age ≥ 18 years and of either sex. - Type I, II, or III skin as assessed by the Fitzpatrick Scale. - Willing to comply with protocol instructions, including allowing all study assessments. - Scheduled to have head or neck non-melanoma skin cancers removed by Mohs micrographic surgery with final wound size of 8 mm to 20 mm in diameter or with 8 mm to 20 mm long axis if not circular. - Acceptable state of health and nutrition, in the opinion of the Investigator. Exclusion Criteria: - History of anaphylaxis, serum sickness, or erythema multiforme reaction to aprotinin, bovine serum albumin or bovine serum proteins, penicillin, streptomycin, or amphotericin B. - Therapy with blood-thinning agents including aspirin within 14 days of the Baseline Visit (these may be resumed post-surgery). - Subjects with platelet or coagulation disorders. - Therapy with another investigational agent within thirty (30) days of Screening, or during the study. - Current systemic therapy with cytotoxic drugs. - Current therapy with chronic (> 10 days) oral corticosteroids. - In the opinion of the Investigator the subject has a current life expectancy of less than 1 year.


NCT ID:

NCT01359735


Primary Contact:

Study Chair
Herbert B Slade, MD
Healthpoint


Backup Contact:

N/A


Location Contact:

Louisville, Kentucky 40217
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: August 31, 2019

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