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Efficacy and Safety of Modified Release Cefpodoxime Formulation in the Treatment of Acute Sinusitis.

Sinusitis Clinical Trial

Official title:
Comparison of the Efficacy and Safety of Immediate (b.i.d) and Modified (q.d.) Release Cefpodoxime Formulations in the Treatment of Acute Sinusitis: a Double-blind, Randomized, Phase III, Non-inferiority Study.

Clinical Trial Summary

The aim of this study is to compare the efficacy and safety of cefpodoxime 200 mg immediate (b.i.d) and cefpodoxime 400 mg modified release (q.d) tablet formulations in the treatment of acute bacterial rhinosinusitis.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03729258
Study type Interventional
Source Neutec Ar-Ge San ve Tic A.S
Contact Neutec RDC
Phone 00905051747902
Email iremkaraman@neutecrdc.com
Status Recruiting
Phase Phase 3
Start date May 15, 2019
Completion date December 1, 2023
View Details
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