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Clinical Trial Details


Research Study Summary

A Phase 2/Phase 3 clinical study for patients with Allergic Bronchopulmonary Aspergillosis

Research Study Title

A Randomized Controlled Trial of Voriconazole in Allergic Bronchopulmonary Aspergillosis


This is a research project to evaluate the efficacy and safety of two different treatment protocols in Allergic bronchopulmonary Aspergillosis.

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Both Male and Female


15 to 65 Years

Overall Status


Lead Sponsor

Postgraduate Institute of Medical Education and Research


36 Months

Facility Type



Both Male and Female ages 15 Years to 65 Years

Inclusion Criteria:

Presence of all the following three criteria:

  • Immediate cutaneous hyperreactivity on aspergillus skin test

  • Elevated total IgE levels > 1000 IU/mL

  • A fumigatus specific IgE levels > 0.35 kUA/L

And, two of the following criteria:

  • Presence of serum precipitating antibodies against A fumigatus

  • Fixed or transient radiographic pulmonary opacities

  • Total eosinophil count > 1000/µL

  • Central bronchiectasis on HRCT

Exclusion Criteria:

  • Failure to give informed consent

  • Intake of glucocorticoids for more than three weeks in the preceding six months

  • Enrollment in another trial of ABPA

  • Any exposure to azoles in the last six months

Site Locations (1)

Country State City Zip Facility and Contact
India Chandigarh 160012 Postgraduate Institute of Medical Education and Research

Ritesh Agarwal, MD, DM
Principal Investigator


Ritesh Agarwal, MD, DM

NCT ID: NCT01621321

Date Last Changed: December 26, 2014

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