Comparison Between 5-aminolevulinic Acid Photodynamic Therapy Versus Cryotherapy for Actinic Keratosis Treatment
Actinic Keratosis
About this trial
This is an interventional treatment trial for Actinic Keratosis focused on measuring Actinic keratosis, Photodynamic therapy, 5-aminolevulinic acid, Cryotherapy
Eligibility Criteria
Inclusion Criteria:
- Patients older than 18 years.
- Patients with actinic keratoses "symmetrical", ie, comparable in the upper limbs ( with the same grade, I, II or III).
- Patients in accordance with informed consent.
Exclusion Criteria:
- Patients with concomitant skin diseases, congenital or acquired (albinism, vitiligo, xeroderma, Gorlin, etc.)
- Immunosuppression (HIV, transplanted patients, etc.)
- Pregnancy or lactation
- Patients who do not agree with the informed consent initially or during the protocol.
- Presence of pigmented lesions near the keratoses.
- Patients with porphyria.
- Patients who have undergone less than 2 months with some kind of treatment for keratosis in the upper limbs.
Sites / Locations
- Barretos Cancer Hospital
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
5-ALA Photodynamic Therapy
Cryotherapy with liquid nitrogen
Topical application of a 2mm of thickness layer of 20% 5-aminolevulinic acid (5-ALA) associated with 20% dimethyl sulfoxide (DMSO) and 3% ethylene diamine acid (EDTA) emulsion, over the actinic keratosis lesion and over a 0,5 cm margin around it. After a 4 hours interval under light protection with plastic film and aluminum foil, the light protection and the emulsion is removed. Then the lesion is lightened with a red (630 nm) incoherent LED lamp AKTILITE CL 128 (PhotoCure ASA, Oslo, Norway) with a total light dose of 37J/cm2.After that dressings are done and kept for 24H, and removed at patient home.
Topical application of liquid nitrogen spray (500ml Cry-ac ® bottle) over the actinic keratosis lesion and over a 0,5 cm margin around it during sufficient time to freeze both the lesion and margin.