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Efficacy and Safety of Voriconazole for Treatment of Invasive Pulmonary Aspergillosis Secondary to COPD: a Multi-center Prospective,Open Cohort Study (VIA-COPD)
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.
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.
Age
30 - 85 years
Sex
ALL
Healthy Volunteers
No
Hangzhou Red Cross Hospital
Hangzhou, Zhejiang, China
Start Date
October 1, 2014
Primary Completion Date
October 1, 2016
Completion Date
December 1, 2016
Last Updated
September 9, 2014
40
ESTIMATED participants
Voriconazole
DRUG
Lead Sponsor
Red Cross Hospital, Hangzhou, China
Collaborators
NCT07477600
NCT07462221
NCT07351929
Data Source & Attribution
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