Healing Effects of HP802-247 Versus Antibiotic Ointment in Mohs Micrographic Surgery Patients

Completed · Phase 2

Conditions studied: Non-melanoma Skin Cancer

In brief

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

Key facts

Study ID

NCT01359735

Run by

Healthpoint

People needed

8

Starts

2011-05-01

Expected to finish

2012-05-01

Last updated by the study team

2017-06-29

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 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.

You may not qualify if…

• 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.

Where it is running

• Derm Research PLC — Louisville, Kentucky, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.