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Comparison of Efficacy of Topical Clobetasol Propionate 0.05% and Topical Tacrolimus 0.1% in the Treatment of Lichen Planus
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Background: Lichen planus (LP) is a papulosquamous cutaneous disorder that manifests as intensely itchy violaceous flat-topped polygonal papules and plaques. To compare the efficacy of topical clobetasol propionate 0.05% versus topical tacrolimus 0.1% in the treatment of LP. Methods: This prospective Comparative Study was conducted at the Dermatology Department, Services Institute of Medical Sciences (SIMS)/Services Hospital, Lahore, from May 1, 2022, to April 30, 2023. Ethical approval was obtained from the institutional review board at the Department of Dermatology, SIMS/Services Hospital, Lahore. A total of 80 patients were selected after fulfilling the selection criteria. The study participants were placed into two groups, A and B. In group A, the patients were advised to use the topical application of clobetasol propionate (0.05%) ointment twice daily. In group B, tacrolimus ointment (0.1%) was used twice daily. Treatment response was assessed at 3 weeks, and then finally efficacy was evaluated at 6 weeks. Results: Treatment efficacy was observed in 34 patients (42.5%). Group A (Clobetasol) demonstrated a significantly higher efficacy of 55% compared to 30% in Group B (Tacrolimus; p = 0.024). Conclusions: The 0.05% clobetasol propionate topical formulation demonstrated superior efficacy in treating LP compared to 0.1% topical tacrolimus. Further validation of these findings through large-scale clinical trials is warranted.
National Society for Biomedical Research Development
Title: Comparison of Efficacy of Topical Clobetasol Propionate 0.05% and Topical Tacrolimus 0.1% in the Treatment of Lichen Planus
Description:
Background: Lichen planus (LP) is a papulosquamous cutaneous disorder that manifests as intensely itchy violaceous flat-topped polygonal papules and plaques.
To compare the efficacy of topical clobetasol propionate 0.
05% versus topical tacrolimus 0.
1% in the treatment of LP.
Methods: This prospective Comparative Study was conducted at the Dermatology Department, Services Institute of Medical Sciences (SIMS)/Services Hospital, Lahore, from May 1, 2022, to April 30, 2023.
Ethical approval was obtained from the institutional review board at the Department of Dermatology, SIMS/Services Hospital, Lahore.
A total of 80 patients were selected after fulfilling the selection criteria.
The study participants were placed into two groups, A and B.
In group A, the patients were advised to use the topical application of clobetasol propionate (0.
05%) ointment twice daily.
In group B, tacrolimus ointment (0.
1%) was used twice daily.
Treatment response was assessed at 3 weeks, and then finally efficacy was evaluated at 6 weeks.
Results: Treatment efficacy was observed in 34 patients (42.
5%).
Group A (Clobetasol) demonstrated a significantly higher efficacy of 55% compared to 30% in Group B (Tacrolimus; p = 0.
024).
Conclusions: The 0.
05% clobetasol propionate topical formulation demonstrated superior efficacy in treating LP compared to 0.
1% topical tacrolimus.
Further validation of these findings through large-scale clinical trials is warranted.
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