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临床试验/JPRN-UMIN000030522
JPRN-UMIN000030522招募中未知

A multicenter, single-arm, prospective study assessing efficacy and safety of the Sirolimus in the Treatment of intractable vascular anomalies - Sirolimus for intractable vascular anomalies

Gifu University0 个研究点目标入组 50 人开始时间: 2017年12月22日最近更新:
适应症

试验速览

阶段
未知
状态
招募中
入组人数
50

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
ot applicable 至 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1)Patients who currently have an uncontrolled infection 2) Uncontrolled diabetes, uncontrolled hypertension, uncontrolled hyperlipidemia, chronic liver disease, or chronic renal disease 3) History of allergy to sirolimus, or additive substance 4) Known history of HIV seropositivity or known immunodeficiency 5) Patients who have undergone surgical resection or interventional radiology procedures for target lesions within 2 weeks 6) Pregnant, probably pregnant, or breast-feeding woman. Patients who do not agree birth control during clinical trial. 7) Patient who is judged inappropriate to participate in this study by the investigators

研究者

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