Impact of Fluocinonide 0,05% in Oral Lichen Planus

Status Recruiting

Clinical Trial Summary

A double-blind placebo-controlled trial is conducted in order to evaluate the efficacy of Fluocinonide 0,05% and determinate the statistical significance of the outcome variables. Oral cavity lichen is a chronic inflammatory condition affecting the mucosa of the oral cavity , which significantly reduces the quality of life of affected individuals.

Clinical Trial Description

A double-blind placebo-controlled study was conducted to evaluate the clinical efficacy of Fluocinonide 0.05% oral gel and determine the statistical significance of outcome variables. 20 patients with Oral Lichen Planus were divided by a randomization system, into two groups: case group treated with Fluocinonide 0.05% oral gel and applied to oral lesions 2 times a day for 1 month and a placebo group as a control group; with 2 months of follow-up. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT06135805
Study type	Interventional
Source	University of Catania
Contact	Gaetano Isola
Phone	0953785652
Email	gaetano.isola@unict.it
Status	Recruiting
Phase	N/A
Start date	October 27, 2020
Completion date	January 3, 2024

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