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Evaluation of the benefit of the addition of 1% topical luliconazole versus topical bland emollient to the systemic itraconazole therapy for the management of disseminated dermatophytosis: A randomised control trial.
Rana, Deval K; Shah, Tithi S; Rohit, Mansi H; Patel, Nayankumar H; Khadela, Avinash D; Oza, Yaksh P; Padhiyar, Jigna K.
Afiliação
  • Rana DK; Department of Pharmacology, L.M. College of Pharmacy, Ahmedabad, Gujarat, India.
  • Shah TS; Department of Pharmacology, L.M. College of Pharmacy, Ahmedabad, Gujarat, India.
  • Rohit MH; Department of Pharmacology, L.M. College of Pharmacy, Ahmedabad, Gujarat, India.
  • Patel NH; GCS Medical College, Hospital and Research Centre, Ahmedabad, Gujarat, India.
  • Khadela AD; Department of Pharmacology, L.M. College of Pharmacy, Ahmedabad, Gujarat, India.
  • Oza YP; GCS Medical College, Hospital and Research Centre, Ahmedabad, Gujarat, India.
  • Padhiyar JK; GCS Medical College, Hospital and Research Centre, Ahmedabad, Gujarat, India.
Mycoses ; 67(1): e13681, 2024 Jan.
Article em En | MEDLINE | ID: mdl-38214352
ABSTRACT

BACKGROUND:

The present epidemic of dermatophytosis in India is marked by an increase in chronic, recurrent and disseminated cases. A combination of oral itraconazole and topical luliconazole is being increasingly utilised by dermatologists in India. The superiority of this combination is not supported by robust clinical trial data.

OBJECTIVE:

We conducted this randomised, open-label, two arms, parallel assignment intervention trial between November 2022 and May 2023 to determine the superiority of topical 1% Luliconazole over bland emollient as adjuvant to systemic Itraconazole therapy in the management of dermatophytosis.

METHOD:

In this study, 135 patients of either sex were randomised to two study cohorts. Major exclusions being concomitant medical illness, use of concomitant medication and substance abuse. Participants were randomly assigned to receive topical bland emollient, (Cohort I, n = 67) or topical luliconazole, (Cohort II, n = 68). Both cohorts received oral itraconazole 200 mg/day (100 mg BID) and levocetirizine 5 mg twice a day as a systemic regime. Clinical and mycological cure at the end of 6 weeks and clinical relapse among cure patients during 10-week follow-up were observed.

RESULTS:

The cure rates for Cohorts I and II at 6 weeks were 50 (74.62%) and 56 (82.35%), (p = .46), respectively. During the 4-week follow-up period, clinical relapses were observed in 16 (32%) of the 50 patients in Cohort I and 12 (21.43%) of the 56 patients in Cohort II (p = .18). Luliconazole cohort shows a significantly higher medical cost (p < .05).

CONCLUSION:

Our study shows a similar cure rate and relapse rate for patients receiving topical Luliconazole versus topical bland emollient as an adjuvant to the systemic itraconazole regime.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Tinha / Itraconazol / Imidazóis Tipo de estudo: Clinical_trials Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Tinha / Itraconazol / Imidazóis Tipo de estudo: Clinical_trials Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article