Overview

Voriconazole for IPA in Chinese Patients With COPD

Status:
Unknown status
Trial end date:
2016-12-01
Target enrollment:
0
Participant gender:
All
Summary
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.
Phase:
Phase 4
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Red Cross Hospital, Hangzhou, China
Collaborators:
First People's Hospital Affiliated to Huzhou University
First People's Hospital of Hangzhou
Hangzhou Hospital of Traditional Chinese Medicine
Ningbo People's Hospital
Second People's Hospital of Hangzhou
Sir Run Run Shaw Hospital
Xiaoshan Hospital
Xiaoshan People's Hospital
Zhejiang Provincial People's Hospital
Zhejiang Provincial People’s Hospital
Treatments:
Voriconazole
Criteria
Inclusion Criteria:

- Cases of invasive pulmonary aspergillosis secondary to COPD

Exclusion Criteria:

- 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