Status:
COMPLETED
Clinical Trial to Evaluate Biafine Cream Versus Standard Care in Subjects With Actinic Keratosis Post Cryotherapy
Lead Sponsor:
Wake Forest University
Conditions:
Actinic Keratosis
Eligibility:
All Genders
50+ years
Phase:
PHASE4
Brief Summary
The purpose of this research study is to evaluate the use of Biafine Cream on wounds created by removal of actinic keratosis using cryotherapy in a clinical setting.
Detailed Description
Subjects were randomized to apply Biafine® to wounds on one forearm and polysporin (standard of care) to wounds on the other. Medications were applied three times a day for 4 weeks to the areas that h...
Eligibility Criteria
Inclusion
- Subject must give written consent.
- Subjects must be \>50 years of age, male or female.
- Subjects must have had cryotherapy treatment of at least one AK's on each forearm in the Dermatology Clinic.
Exclusion
- Subjects age \<50 years of age.
- Subjects with known allergy or sensitivity to topical Biafine or polysporin ointment.
- Inability to complete all study-related visits.
- Introduction of any other prescription medication, topical or systemic, for AK while participating in the study.
- Subjects using other topical agent's glycolic acid products, alpha-hydroxy acid products, retinoids and chemical peel agents in the treatment areas while on study.
Key Trial Info
Start Date :
October 1 2006
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
February 1 2008
Estimated Enrollment :
20 Patients enrolled
Trial Details
Trial ID
NCT00695578
Start Date
October 1 2006
End Date
February 1 2008
Last Update
December 31 2018
Active Locations (1)
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1
Wake Forest University Health Sciences Dermatology
Winston-Salem, North Carolina, United States, 27157