跳至主要内容
临床试验/NCT07044141
NCT07044141进行中(未招募)1 期

Efficacy of Oral Tofacitinib in Combination With Narrow Band UVB in the Treatment of Vitiligo

Lahore General Hospital1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2025年3月1日最近更新:
干预措施
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
20
试验地点
1
主要终点
VASI improvement upto 50%

研究概览

简要总结

20 patients will be enrolled. All were given narrowband UVB . 10 wil be give oral azathriopfine . 10 will be given tofacitinib

详细描述

Total 20 patients will be enrolled. All were given narrowband UVB . 10 wil be give oral azathriopfine 50mg twice daily. 10 will be given tofacitinib 5mg twice daily. For 6 months

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • patient of vitiligo with any VASI both genders 18 to 60yrs

排除标准

  • pregnancy/lactation Hyerlipidrmia Patient on immunemodulator Histry pf tuberculosis Immunocompromised patients

研究组 & 干预措施

Group A

Active Comparator

Azathioprine is an immunomodulator used in treatment of vitiligo

干预措施: Azathioprine (Drug)

Group B

Active Comparator

Tofacitinib It is a Janu kinase pathway inhibitor

干预措施: Tofacitinib (Drug)

结局指标

主要结局

VASI improvement upto 50%

时间窗: 6 months

Study will be considered efficacious if 50% improvement in VASI from baseline is seen by end of 6 months of study

次要结局

未报告次要终点

研究者

申办方类型
Other Gov
责任方
Principal Investigator
主要研究者

Dr ayesha wahid

Dr saadiya siddiqui

Lahore General Hospital

研究点 (1)

Loading locations...

相似试验