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A Study to Evaluate the Clinical and Microbial Efficacy and Safety of 1.0 % AzaSite Compared to Vehicle in the Treatment of Bacterial Conjunctivitis

NCT00105534 Phase 3 COMPLETED Results posted

The purpose of this study is to evaluate the clinical and microbial efficacy and safety of AzaSite compared to vehicle for bacterial conjunctivitis. Adults and children one year of age and older with bacterial conjunctivitis in at least one eye may be eligible. Subjects will be randomly assigned to receive either 1.0 % AzaSite or Vehicle. Three visits will be required for this study.

Details

Lead sponsorMerck Sharp & Dohme LLC
PhasePhase 3
StatusCOMPLETED
Enrolment685
Start date2004-07
Completion2006-01

Conditions

Interventions

Primary outcomes

Countries

United States