Status:

UNKNOWN

Efficacy and Safety of Caspofungin for Invasive Pulmonary Aspergillosis Underlying Chronic Obstructive Pulmonary Disease

Lead Sponsor:

The First Affiliated Hospital of Guangzhou Medical University

Collaborating Sponsors:

Merck Sharp & Dohme LLC

Conditions:

Invasive Pulmonary Aspergillosis

Chronic Obstructive Pulmonary Disease

Eligibility:

All Genders

18+ years

Phase:

PHASE4

Brief Summary

The investigators propose to study the efficacy and safety of three-week antifungal therapy with caspofungin in hospitalized patients with proven or probable IPA underlying chronic obstructive pulmona...

Detailed Description

Recently, there has been increasing appreciation of chronic obstructive pulmonary disease (COPD) as an important risk factor of invasive pulmoanry aspergillosis (IPA). However, clinical data on the mo...

Eligibility Criteria

Inclusion

  • Proven invasive pulmonary aspergillosis
  • Probable invasive pulmonary aspergillosis
  • Hospitalized in respiratory wards
  • Not having received an empirical antifungal therapy for 72h before inclusion

Exclusion

  • A history of allergy to echinocandins
  • Severe renal failure, severe hepatic insufficiency
  • Inadequately treated bacterial infection
  • Documented HIV infection
  • Status of pregnancy or lactation

Key Trial Info

Start Date :

January 1 2012

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

November 1 2014

Estimated Enrollment :

40 Patients enrolled

Trial Details

Trial ID

NCT01499433

Start Date

January 1 2012

End Date

November 1 2014

Last Update

January 23 2014

Active Locations (1)

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Guangzhou Institute of Respiratory Diseases

Guangzhou, Guangdong, China, 510120