Comparative evaluation of the efficacy of Nigella sativa (75% v/v) cream and clobetasol propionate (0.05% w/w) gel in oral lichen planus-a double-blinded randomized control trial

被引:4
作者
Kumar, S. Lokesh [1 ]
Naik, Zameera [2 ]
Panwar, Arun [2 ]
Sridhar, M. [2 ]
Keluskar, Vaishali [2 ]
Kumar, Ram Surath [3 ]
机构
[1] Saveetha Inst Med & Tech Sci SIMATS, Saveetha Dent Coll & Hosp, Dept Oral Med Radiol & Special Care Dent, 162 Poonamalle High Rd, Chennai 600077, Tamil Nadu, India
[2] KLE Acad Higher Educ & Res, KAHERs KLE Vishwanath Katti Inst Dent Sci, Dept Oral Med & Radiol, JNMC Campus, Belagavi 590010, Karnataka, India
[3] KLE Acad Higher Educ & Res, KAHERs KLE Vishwanath Katti Inst Dent Sci, Dept Publ Hlth Dent, JNMC Campus, Belagavi 590010, Karnataka, India
来源
ORAL AND MAXILLOFACIAL SURGERY-HEIDELBERG | 2024年 / 28卷 / 01期
关键词
Lichen planus; oral; Precancerous conditions; Pain; Clobetasol; Nigella sativa; Randomized control trial; Affordable medicines; TRIAMCINOLONE ACETONIDE 0.1-PERCENT; ALOE-VERA; CURRENT CONTROVERSIES; CLINICAL MANAGEMENT; THYMOQUINONE; OIL;
D O I
10.1007/s10006-022-01130-6
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Objectives The aim of this study is to evaluate and compare the efficacy of Nigella sativa (75% v/v) cream and clobetasol propionate (0.05% w/w) gel for the management of oral lichen planus (OLP).Study design Sixty clinically diagnosed cases of OLP were stratified into moderate cases or severe cases based on burning sensation before getting allocated to group I receiving Nigella sativa cream and group II receiving clobetasol propionate gel, two times a day for 45 days. Patients were examined every 15 days for a change in burning sensation and size of the lesion using the numeric pain rating scale (NRS) and a standard Vernier caliper, respectively. Statistical tests including Mann- Whitney U, Wilcoxon signed-rank, Friedman's, Dunn's post hoc, unpaired t, paired t, one-way repeated measures ANOVA, and Bonferroni's post hoc were applied.Results There was a statistically significant reduction in the burning sensation as well as the size of the lesion in both groups (P <= 0.05). There was an 87.8% (moderate cases) and 85.7% (severe cases) reduction in the mean NRS scores on the 45th day in group I when compared to the 96.5% (moderate cases) and 93.48% (severe cases) in group II. There was a 92.9% (moderate cases) and 90.7% (severe cases) reduction in the size of the lesion in group I when compared to the 92.6% (moderate cases) and 93.1% (severe cases) in group II.Conclusion The topical application of Nigella sativa cream was effective and comparable to clobetasol propionate 0.05% gel in the management of OLP, without any side effects. Hence, this study recommends the use of topical Nigella sativa cream therapy in the management of OLP.Clinical relevance The current mainstay of treatment for OLP is the administration of topical or systemic corticosteroids, which are known to cause side effects, demanding a search for an alternative. Nigella sativa oil cream could be a safe, promising, cost-effective, adjunctive, or alternative modality. Clinical trial registration number: CTRI/2020/07/026745 (India).
引用
收藏
页码:225 / 234
页数:10
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