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临床试验/NCT02234739
NCT02234739Unknown4 期

Efficacy and Safety of Voriconazole for Treatment of Invasive Pulmonary Aspergillosis Secondary to COPD: a Multi-center Prospective,Open Cohort Study (VIA-COPD)

Red Cross Hospital, Hangzhou, China1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2014年10月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
发起方
入组人数
40
试验地点
1
主要终点
success rate of voriconazole antifungal treatment

研究概览

简要总结

voriconazole is recommended as first-line therapy for invasive pulmonary aspergillosis, however the efficacy and safety of voriconazole for treating invasive pulmonary aspergillosis secondary to COPD is not clear. This study aims to investigate the effectiveness and tolerability of intravenous voriconazole for treatment of invasive pulmonary aspergillosis in Chinese patients with COPD, by monitoring changes in clinical symptoms, eradication of aspergillus, improvement of chest imaging as well as record of possible adverse reactions following 2-week intravenous instillation of voriconazole.

详细描述

This is a multiple-center open-label clinical trial to study the efficacy and safety of voriconazole for treating invasive pulmonary aspergillosis secondary to COPD in Chinese patients.The primary endpoint is treatment success rate as defined by improvement of symptoms related to invasive pulmonary asperillosis, secondary endpoints include the mortality, the eradication of sputum asperillus and profile of adverse reactions following intravenous instillation of voriconazole.

研究设计

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

入排标准

年龄范围
30 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Cases of invasive pulmonary aspergillosis secondary to COPD

排除标准

  • Use of voriconazole or itraconazole or amphotericin B or caspofungin or micafungin within 4 weeks prior to enrollment
  • Known allergy to voriconazole
  • Severe impairment of live or kidney function
  • Septic shock
  • Unwilling to sign informed consent

研究组 & 干预措施

active treatment

Experimental

Chinese patients with invasive pulmonary aspergillosis treated by voriconazole, who has COPD as underlying condition

干预措施: Voriconazole (Drug)

结局指标

主要结局

success rate of voriconazole antifungal treatment

时间窗: 2-week

treatment success if defined as improve of symptoms related to invasive pulmonary aspergillosis, such as fever, wheezing, chest pain, dyspnea, and hemoptysis

次要结局

  • adverse reactions following voriconazole treatment(2-week)

研究者

发起方
Red Cross Hospital, Hangzhou, China
申办方类型
Other
责任方
Principal Investigator
主要研究者

caichuang

professor

Red Cross Hospital, Hangzhou, China

研究点 (1)

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