Your browser doesn't support javascript.
loading
Role of the ACTH test and estimation of a safe dose for high potency steroids in vitiligo: A prospective randomized study.
de la Fuente-García, Alberto; Gómez-Flores, Minerva; Mancillas-Adame, Leonardo; Ocampo-Candiani, Jorge; Welsh-Lozano, Oliverio; Pérez, Jesús Zacarías Villarreal; González-González, José Gerardo; Lavalle-González, Fernando.
  • de la Fuente-García A; Department of Dermatology, Dr. José E. González University Hospital, Monterrey, Nuevo León, México.
  • Gómez-Flores M; Department of Dermatology, Dr. José E. González University Hospital, Monterrey, Nuevo León, México.
  • Mancillas-Adame L; Department of Endocrinology, Dr. José E. González University Hospital, Monterrey, Nuevo León, México.
  • Ocampo-Candiani J; Department of Dermatology, Dr. José E. González University Hospital, Monterrey, Nuevo León, México.
  • Welsh-Lozano O; Department of Dermatology, Dr. José E. González University Hospital, Monterrey, Nuevo León, México.
  • Pérez JZ; Department of Endocrinology, Dr. José E. González University Hospital, Monterrey, Nuevo León, México.
  • González-González JG; Department of Endocrinology, Dr. José E. González University Hospital, Monterrey, Nuevo León, México.
  • Lavalle-González F; Department of Endocrinology, Dr. José E. González University Hospital, Monterrey, Nuevo León, México.
Indian Dermatol Online J ; 5(2): 117-21, 2014 Apr.
Article en En | MEDLINE | ID: mdl-24860741
ABSTRACT

BACKGROUND:

Topical corticosteroids are used as first line of therapy for vitiligo, although side effects such as adrenal insufficiency are possible.

OBJECTIVES:

To establish the role of ACTH test before, during, and after treatment with high potency topical steroids; to determine if adrenal insufficiency occurs secondary to the use of high potency topical steroids in patients with vitiligo and intact cutaneous barrier; and also to determine response to treatment and side effects. MATERIALS AND

METHODS:

Forty-four adults with non-segmental vitiligo affecting 20% or less of the body surface area were included and randomized to receive topical clobetasol propionate 0.05% cream (group 1) or placebo (group 2) for 12 weeks, with a maximum dose of 50 g per week. The placebo group was crossed over after week 6 and started on clobetasol until completion of the study. Serum cortisol levels with the 1 µg ACTH test were determined at baseline and on weeks 6 and 12.

RESULTS:

No adrenal insufficiency was detected nor statistical significance was achieved when comparing cortisol levels between and within the groups at baseline and weeks 6 and 12. Group 1 had a better response to therapy but with more side effects.

CONCLUSIONS:

Doses of 50 g or less per week of clobetasol during a period of 12 weeks are safe on adult vitiligo patients, although local side effects are possible. Repigmentation rates were incomplete with single steroid therapy, making combined therapy a better option.
Palabras clave

Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Clinical_trials Idioma: En Año: 2014 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Clinical_trials Idioma: En Año: 2014 Tipo del documento: Article