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Clinical Trial Summary

The study should create data for the selection of a clinically relevant primary endpoint to assess the efficacy and safety of Buparid/PARI SINUS as compared to Budes Nasal Spray in the therapy of chronic rhinosinusitis (CRS) with polyposis nasi in adult patients. Ideally, the selected parameter should allow a correlation between an objective methodology and the clinical outcome of the study patients.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01946711
Study type Interventional
Source Pari Pharma GmbH
Contact
Status Completed
Phase Phase 1/Phase 2
Start date August 28, 2013
Completion date June 21, 2021

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