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Clinical Trial Summary

Since abnormal keratinocyte (KC) proliferation and differentiation as well as defective E cadherin expression were reported in vitiligo lesions, the investigators set to study the potential efficacy of combining Retinoids, which are known to improve KC proliferation and differentiation and increase the expression of adhesion molecules, with narrowband UVB in the treatment of vitiligo.


Clinical Trial Description

• Twenty patients with generalized vitiligo will be included in this study. All patients will be subjected to: - Clinical evaluation: - An informed written consent. - History taking include age, previous treatment, disease activity - Clinical examination including Vitiligo Area Scoring Index (VASI) and Vitiligo Disease Activity Score (VIDA) - Photography (before starting the treatment and every 2 weeks till the end of the study) Laboratory evaluation: - 2 mm punch skin biopsies will be taken from vitiligo patients, 1 from lesional and the other from perilesional skin before treatment. - The patients will be randomly assigned to two groups: Group A: patients will receive three NB-UVB sessions per week for 48 sessions. Group B: patients will receive three NB-UVB sessions per week for 48 sessions combined with acitretin in a dose of 0.3mg/kg/day daily. - Controls: 20 individuals age and sex matched will be biopsied from the skin of their abdominoplasty surgery. - Another two 2 mm punch skin biopsies will be taken from lesional and perilesional skin at the onset of repigmentation if repigmentation starts before completion of the 48 treatment session or after completion of the treatment period if repigmentation does not occur. - .All biopsies from patients and controls will be stained Immunohistochemically by anti-E cadherin antibody. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04245319
Study type Interventional
Source Cairo University
Contact Noha A. Saleh, M.Sc
Phone +201222177210
Email noushy2938@gmail.com
Status Recruiting
Phase N/A
Start date January 1, 2020
Completion date December 1, 2021

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