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A Single-Center, Randomized, Masked Study Comparing the Concentration of Besifloxacin, Gatifloxacin, and Moxifloxacin in Human Conjunctiva After a Single Topical Instillation

NCT00905762 Phase 1 COMPLETED

The purpose of this study is to assess the concentration of besifloxacin compared to gatifloxacin and moxifloxacin in human conjunctival tissue, following a single drop of the drug instilled topically into the study eye. Conjunctival biopsies will be performed at specified time points, followed by the use of loteprednol etabonate/tobramycin ophthalmic suspension four times a day for 5 days.

Details

Lead sponsorBausch & Lomb Incorporated
PhasePhase 1
StatusCOMPLETED
Enrolment119
Start date2009-03
Completion2009-04

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Interventions

Primary outcomes

Countries

United States