The purpose of this study is to determine if Levulan photodynamic therapy (PDT) is safe and effective in the treatment of actinic keratoses (AK) on the face, following treatment with liquid nitrogen cryotherapy.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
166
20% ALA applied to face for one hour prior to 10 J/cm2 blue light
Levulan Kerastick containing vehicle ingredients only. Vehicle solution applied to face one hour prior to 10 J/cm2 blue light
10 J/cm2 blue light delivered at 10 mW/cm2
UCSD Dermatology
San Diego, California, United States
Therapeutics Clinical Research
San Diego, California, United States
Altman Dermatology Associates
Arlington Heights, Illinois, United States
Shideler Clinical Research Center
Carmel, Indiana, United States
Total Number of AKs in Treatment Area
Count of observed lesions in the treatment area, which include lesions that recurred after on-study cryotherapy as well as newly occurring lesions. AK lesions in the treatment area at baseline (maximum of 2) were excluded for this endpoint.
Time frame: Week 52
Proportion of Subjects With 0 AKs
Normalized based on number of lesions present at Baseline
Time frame: Week 4
Subject Satisfaction Score
Subject satisfaction score 1. = Excellent (very satisfied) 2. = Good (moderately satisfied) 3. = Fair (slightly satisfied) 4. = Poor (not satisfied at all) Unknown
Time frame: Week 52
Proportion of Subjects With 0 AKs
Normalized based on number of lesions present at Baseline
Time frame: Week 12
Proportion of Subjects With 0 AKs
Normalized based on number of lesions present at Baseline
Time frame: Week 24
Proportion of Subjects With 0 AKs
Normalized based on number of lesions present at Baseline
Time frame: Week 36
Proportion of Subjects With 0 AKs
Normalized based on number of lesions present at Baseline
Time frame: Week 52
Recurrence Rate
Recurrence rate of all lesions that were complete responses following on-study cryotherapy (at Visit 3/Baseline).
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Liquid nitrogen cryotherapy by standard of care method to all visible/palpable actinic keratosis (AK) lesions at screening.
Sadick Research Group
New York, New York, United States
Tennessee Clinical Research Center
Nashville, Tennessee, United States
Suzanne Bruce and Associates, P.A.,The Center for Skin Research
Houston, Texas, United States
Virginia Clinical Research, Inc.
Norfolk, Virginia, United States
Time frame: Week 52
Duration of Response
Duration of response is the elapsed number of weeks from the Baseline visit until a lesion recurred or Week 52, whichever comes first
Time frame: within 52 weeks after Baseline