Clinical Trials Directory

Trials / Completed

CompletedNCT06042010

Oral Zinc Supplement as Adjunctive Therapy for Erosive Oral Lichen Planus

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

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
22 (actual)
Sponsor
Hams Hamed Abdelrahman · Academic / Other
Sex
All
Age
25 Years
Healthy volunteers
Not accepted

Summary

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.

Conditions

Interventions

TypeNameDescription
DRUGOral zinc supplementpatients received oral Zinc picolinate 50mg for 6 weeks as single morning dose along with 0.1%
DRUGtriamcinolone acetonide Oral pastepatients will received 0.1%triamcinolone acetonide Oral paste twice daily alone for 6weeks.

Timeline

Start date
2023-01-05
Primary completion
2023-02-14
Completion
2023-02-14
First posted
2023-09-18
Last updated
2023-09-18

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT06042010. Inclusion in this directory is not an endorsement.