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临床试验/NCT04056962
NCT04056962招募中2 期

Tacrolimus for the Treatment of Superficial Kaposiform Hemangioendothelioma and Tufted Angioma:a Randomized Controlled Study

West China Hospital1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2019年9月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
招募中
入组人数
50
试验地点
1
主要终点
reduction in the size of the lesion

研究概览

简要总结

The aim of this study was to evaluate the efficacy and safety of topical application of tacrolimus at different concentrations for superficial Kaposiform hemangioendothelioma (KHE) and tufted angioma (TA).

详细描述

Kaposiform hemangioendothelioma (KHE) and tufted angiomas (TA) are rare vascular tumors, which are apparent predominantly in infancy or early childhood. Currently, no standard treatment regimens exist for KHE/TA. The aim of this study was to evaluate the efficacy and safety of topical application of tacrolimus at different concentrations for superficial Kaposiform hemangioendothelioma (KHE) and tufted angioma (TA).

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
Single (Outcomes Assessor)

入排标准

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

入选标准

  • Children with superficial Kaposiform hemangioendothelioma (KHE) and tufted angioma (TA)

排除标准

  • Hypersensitivity to Tacrolimus Mucosal Kaposiform hemangioendothelioma (KHE) and tufted angioma (TA)

研究组 & 干预措施

patients treated with tacrolimus 0.03% ointment

Experimental

patients treated with tacrolimus 0.03% ointment

干预措施: Tacrolimus ointment (Drug)

patients treated with tacrolimus 0.1% ointment

Active Comparator

patients treated with tacrolimus 0.1% ointment

干预措施: Tacrolimus ointment (Drug)

结局指标

主要结局

reduction in the size of the lesion

时间窗: 2.5 years

Therapeutic effect is evaluated by reduction in the size of the tumor measured by centimeters.

次要结局

  • Rate of Adverse events(2.5 years)

研究者

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

Yi Ji

Doctor of Philosophy, Doctor of Medicine

West China Hospital

研究点 (1)

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