Dr Michaels® (Soratinex®) product for the topical treatment of psoriasis: a Hungarian/Czech and Slovak study
Language English Country Italy Media print
Document type Clinical Trial, Journal Article
PubMed
27498657
PII: 7
Knihovny.cz E-resources
- MeSH
- Administration, Topical MeSH
- Coal Tar administration & dosage adverse effects therapeutic use MeSH
- Child MeSH
- Adult MeSH
- Emulsifying Agents administration & dosage adverse effects therapeutic use MeSH
- Middle Aged MeSH
- Humans MeSH
- Adolescent MeSH
- Young Adult MeSH
- Plant Oils administration & dosage adverse effects therapeutic use MeSH
- Skin Care adverse effects methods MeSH
- Psoriasis drug therapy pathology MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Treatment Outcome MeSH
- Check Tag
- Child MeSH
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Adolescent MeSH
- Young Adult MeSH
- Male MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Clinical Trial MeSH
- Geographicals
- Czech Republic MeSH
- Hungary MeSH
- Slovakia MeSH
- Names of Substances
- Coal Tar MeSH
- Emulsifying Agents MeSH
- Plant Oils MeSH
Psoriasis is a chronic inflammatory T cell-mediated skin disease, affecting about 2% of Hungarian population. Genetic predisposition as well as environmental triggering factors, and innate immune processes play a role in its etiology. Treatment of psoriasis during the initial stages and first years of disease tend to be conservative and frequently based on topical agents. The aim of this study was to investigate and to describe the efficacy and safety of Dr Michaels® (Soratinex®) skin-care products for the topical treatment of stable chronic plaque psoriasis in a Hungarian population. Two-hundred-and-eight-six (120 female/166 male) patients, aged 10-80 years old (mean age 43 years) with mild to moderate plaque psoriasis had participated in the study. The products, including cleansing gel containing a coal tar solution, herbal oils and emulsifiers, were used twice daily and in the same manner for all the skin lesions. The study period was eight weeks. Assessment, using the Psoriasis Activity Severity Index (PASI) scores and photographic analysis, was done 2 weeks before treatment, at time 0, and after 2, 4, 6 and 8 weeks. Patients improvement was determined by the percentage reduction of the PASI scores. Side effects and tolerability were also evaluated. After 8 weeks treatment course, 46 patients had a moderate improvement, with the regression of 25-50% of skin lesions; 77 patients showed a good improvement, with the resolution of 51-75% of lesions. Another 115 patients had an outstanding improvement, with the regression of 76-98.9% of lesions. Only 13 patients did not achieve an improvement of psoriasis. Fifteen patients experienced folliculitis, which resolved after cessation of treatment. Seven patients worsened and discontinued treatment. Thirteen patients dropped out because of non-compliance. Our investigation demonstrates that Dr Michaels® (Soratinex®) products, an Australian treatment, can be used successfully in the treatment of stable chronic plaque psoriasis.
Chair of Dermatology University of Rome G Marconi Rome Italy
Department of Nuclear Physics Sub nuclear and Radiation G Marconi University Rome Italy
Dermatological Department University of Pisa Pisa Italy
PRO SANUM Ltd Sanatorium of Prof Novotný Štěpánská Prague 1 Czech Republic
Psoriasis and Skin Clinic Melbourne Australia
University B 1 S Group of Institutions Punjab Technical University Punjab India