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临床试验/NCT00372307
NCT00372307已完成2 期

Efficacy and Safety of Pimecrolimus for the Treatment of Vitiligo Vulgaris

University Hospital, Ghent2 个研究点 分布在 1 个国家目标入组 26 人开始时间: 2004年5月最近更新:
适应症
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
26
试验地点
2
主要终点
Repigmentation percentage of the reference lesion after 6 months.

研究概览

简要总结

Patients with vitiligo vulgaris are treated with Pimecrolimus twice a day during 6 months. After a baseline visit, patient returns for a control visit after 3 and 6 months of treatment. One reference lesion is clinically evaluated with pictures.

研究设计

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

入排标准

年龄范围
6 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Active or stable vitiligo vulgaris
  • lesions at head or neck + maximum 10% lesions at the rest of the body

排除标准

  • Topica during last 2 weeks
  • Photo(chemo)therapy during last 4 weeks
  • Segmentary vitiligo

结局指标

主要结局

Repigmentation percentage of the reference lesion after 6 months.

次要结局

  • Number of patients with repigmentation after 3 and 6 months.
  • Repigmentation percentage of the reference lesion after 3 months.
  • Adverse events (month 3 and 6).

研究者

申办方类型
Other

研究点 (2)

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