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DOI 10.1111/j.1365-4632.2004.02130.x

Медицинская библиотека · International journal of dermatology · 2005

Adapalene vs. metronidazole gel for the treatment of rosacea.

Altinyazar H Cevdet, Koca Rafet, Tekin Nilgün Solak, Eştürk Emel

Клиническое исследованиеСравнительное исследованиеСтатьяРандомизированное исследованиеПеревод пока не подготовлен

Аннотация

BACKGROUND

Rosacea is a common, chronic dermatosis that requires long-term therapy. Oral isotretinoin and topical and/or oral antibiotics are effective, but their usage may be limited due to side-effects.

OBJECTIVE

The goal of the study was to compare the efficacy of topical adapalene gel (0.1%) and topical metronidazole gel (0.75%) in the treatment of patients with papulopustular rosacea.

METHODS

This study included 55 patients with papulopustular rosacea. Diagnostic efforts were focused on clinical and histological features. Patients were randomly assigned to the adapalene (n = 30) and metronidazole (n = 25) groups. Sunlight protection factor 20 cream was used to protect all patients from sunlight. The characteristics and numbers of inflammatory papules, pustules, erythema and telangiectasia were scored at baseline and after 2, 4, 8 and 12 weeks. Side-effects were recorded at each visit.

RESULTS

Fifty patients, 27 in the adapalene group and 25 in the metronidzaole group, completed the study. Significant reductions in the total number of inflammatory lesions were found in the adapalene group compared with the metronidazole group. There was no significant difference in the scores of erythema and telangiectasia in the adapalene group. However, a significant reduction in erythema was seen in the metronidazole group.

CONCLUSIONS

Adapalene gel is well tolerated and can be used as an alternative for topical treatment of papulopustular rosacea.

Для цитирования: Altinyazar H Cevdet, Koca Rafet, Tekin Nilgün Solak, Eştürk Emel. Adapalene vs. metronidazole gel for the treatment of rosacea.. International journal of dermatology. 2005. DOI: 10.1111/j.1365-4632.2004.02130.x.

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