跳至主要内容
临床试验/CTRI/2023/01/048849
CTRI/2023/01/048849已完成不适用

A retrospective study to evaluate efficacy and safety of oral tofacitinib in vitiligo and its variants

NA1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2023年10月1日最近更新:

试验速览

阶段
不适用
状态
已完成
发起方
NA
入组人数
40
试验地点
1
主要终点
To assess improvement in VASI from baseline

研究概览

简要总结

Vitiligo is a chronic autoimmune condition associatedwith marked psychological distress, especially in our country owing to thedarker skin types. There is a growing need for targeted therapies in vitiligofor its effective clearance. JAK (Janus kinase) inhibitors act by inhibitingIFN (Interferon) gamma signalling which is the main cytokine implicated in melanocytedestruction(1). However, data regarding ideal dosing, efficacy and long-term safety oforal tofacitinib in the Indian population is lacking. Through our study, wehope to bridge this gap and aid in creating a standardised protocol for the useof oral tofacitinib in vitiligo.

研究设计

研究类型
Interventional
分配方式
Not Applicable
盲法
Not Applicable

入排标准

年龄范围
18.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • All clinically diagnosed cases of different variants of vitiligo 2.Patients who were started on oral tofacitinib for vitiligo.

排除标准

  • •Patients receiving other systemic immunosuppressive drugs.

结局指标

主要结局

To assess improvement in VASI from baseline

时间窗: After 6 months

次要结局

  • 1.To assess number of patients achieving VASI 50/75/90 at the end of treatment follow-up period(2.To assess change in BSA (Body Surface Area) from baseline)

研究者

发起方
NA
申办方类型
Private hospital/clinic

研究点 (1)

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