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临床试验/CTRI/2022/12/048004
CTRI/2022/12/048004已完成不适用

A comparative study evaluating the efficacy of oral tofacitinib versus oral mini pulse of corticosteroids in alopecia areata.

All India Institute of Medical Sciences, Jodhpur1 个研究点 分布在 1 个国家目标入组 82 人开始时间: 2022年12月12日最近更新:

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
82
试验地点
1
主要终点
Change in SALT Score.

研究概览

简要总结

Alopecia areata (AA) is an autoimmune disorder which usually presents as non-scarring patches of hair loss.  AA comprises nearly one-fourth of all cases of hair loss. It usually starts in childhood but can affect individuals of any age. Unfortunately, there is no cure and no universally proven treatment that induces sustained remission for AA. Various treatment modalities used in alopecia areata are corticosteroids, immunotherapy and PUVA. Out of these, corticosteroids seem to be the most common treatment, however, the use of corticosteroids is associated with many adverse effects. In addition to the adverse effects, the response rate to the steroids varies greatly among patients. Several studies indicate that inhibition of the JAK pathway could be a promising treatment option for severe or progressive alopecia areata. Various retrospective studies and case series show a very promising response of Tofacitinib in the treatment of AA. However, a very few prospective studies have been conducted to compare the efficacy of tofacitinib with conventional treatment used in AA. In this study we will compare the efficacy of tofacitinib versus oral steroid in the management of alopecia areata.

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Outcome Assessor Blinded

入排标准

年龄范围
14.00 Year(s) 至 50.00 Year(s)(—)
性别
All

入选标准

  • Clinically diagnosed patient of alopecia areata with more than 20% scalp hair loss or rapidly progressive disease.
  • Age >14 years and <50 years.

排除标准

  • Previously treated patients within 2 weeks of topical therapy or 4 weeks of systemic therapy
  • Patients who have hepatic impairment
  • Patients with abnormal blood counts (lymphocyte <500cell/mm3 or neutrophils <1000 cell/mm3)
  • Pregnant and lactating women.
  • Immunocompromised patients or if is a K/C/O Hepatitis B,C,or HIV
  • Patient having an active infection, any systemic illness, uncontrolled diabetes mellitus or hypertension.

结局指标

主要结局

Change in SALT Score.

时间窗: At 4 weeks, 8 weeks, 12 weeks and 16 weeks.

次要结局

  • 1. Physician global assessment score(2. Patient global assessment score)

研究者

发起方
All India Institute of Medical Sciences, Jodhpur
申办方类型
Government medical college

研究点 (1)

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