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临床试验/NCT06042010
NCT06042010已完成不适用

Efficacy of Oral Zinc Supplement as an Adjunctive Therapy for Erosive Oral Lichen Planus (a Randomized, Controlled Clinical Trial)

Hams Hamed Abdelrahman1 个研究点 分布在 1 个国家目标入组 22 人开始时间: 2023年1月5日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
22
试验地点
1
主要终点
Change in oral lesions

研究概览

简要总结

Lichen Planus (LP) is a chronic mucocutaneous inflammatory disease and considered as T-cell mediated autoimmune disorder.

Zinc is a potent antioxidant micronutrient that contributes to the proper functioning of the antioxidant defense system. In addition, this mineral protects cells against inflammation by oxidative stress, because it acts in the stabilization of cell membrane. It also maintains macrophage and neutrophil functions, natural killer cell activity, and complement activity.

Matrix metalloproteinases (MMPs) are a family of zinc-containing endopeptidases and have the main function of proteolytic degradation of connective tissue matrix proteins. Zinc prevents (MMP-1) activation and inhibition of the T-cell accumulation in (OLP) through inhibiting of (MMP-9).

Aim of the study: To evaluate and compare the efficacy of adding oral zinc supplementation 50 mg to 0.1%Triamcinolone orabase (TA)versus 0.1%Triamcinolone orabase alone on the healing of erosive OLP.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
25 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • All patients involved in this clinical trial will have symptomatic OLP

排除标准

  • Smokers or tobacco users will be excluded from this clinical trial.
  • Pregnant and lactating females.
  • Any patient that has history of cancer, kidney, liver or other autoimmune disease will be excluded from this study.
  • Patients showing dysplastic changes in their confirmatory biopsy specimen will be also excluded.
  • Any patients presenting with extra oral lichen planus lesions will be excluded.
  • Suspicious lesions of both lichenoid contact reaction and lichenoid drug reaction lesions will be excluded.
  • Vitamin administration intake within the last 3 months

研究组 & 干预措施

Test group

Experimental

干预措施: Oral zinc supplement (Drug)

control group

Active Comparator

干预措施: triamcinolone acetonide Oral paste (Drug)

结局指标

主要结局

Change in oral lesions

时间窗: Baseline, 6 weeks, 12 weeks

Thongprasom scoring system will be used for the measurement of objective outcomes; score 5 was assigned to patients having white striae with erosive areas \>1 cm2, score 4 assigned to patients with white striae and erosive areas \<1 cm2, score 3 assigned to those having white striae and atrophic areas \>1 cm2, score 2 assigned to those having white striae and atrophic areas \<1 cm2, score 1 assigned to those having only white striae, and score 0 assigned to normal mucosa.

Change in MMP-9 level

时间窗: Baseline, 6 weeks, 12 weeks

Whole unstimulated saliva will be collected from all participants

次要结局

  • Change in pain(Baseline, 6 weeks, 12 weeks)

研究者

发起方
Hams Hamed Abdelrahman
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Hams Hamed Abdelrahman

Assistant lecturer of DPH and Clinical statistician

Alexandria University

研究点 (1)

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