The effect of epigallocatechin gallate loaded nanostructured lipid carriers on oral lichen planus

Phase 3

Recruiting

• Conditions: oral lichen planus.; Other lichen planus; L43.8

• Registration Number: IRCT20230823059238N1
• Lead Sponsor: Tabriz University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 16 October 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 46

Inclusion Criteria

Definite Diagnosis of Lichen Planus via Clinial criteria and Histopathology
approvement Range of 17 to 70 years old

Exclusion Criteria

Pregnancy or breastfeeding
Usage of Immuno supressor Drugs
Any treatment that has been done for these injuries

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Severity of pain. Timepoint: Before the start of the intervention and 2 and 4 weeks after the intervention. Method of measurement: The severity of pain will be evaluated through visual analogue scale (VAS).;The size of lesions. Timepoint: Before the start of the intervention and 2 and 4 weeks after the intervention. Method of measurement: The size of lesions will be measured with paper lace.;The appearance of lesions. Timepoint: Before the start of the intervention and 2 and 4 weeks after the intervention. Method of measurement: The appearance of lesions will be measured by Thongprasom scale and includes 6 grades: zero = perfectly healthy, 1 = mild white lines without inflammatory regions, 2 = white lines with atrophic regions smaller than 1 cm2, 3 = white lines with atrophic regions larger than 1 cm2, 4 = white lines accompanied with erosive regions less than 1 cm2, 5 = white lines with erosive areas larger than 1 cm2 .