Clinical Trials Directory

Trials / Completed

CompletedNCT00905762

Concentration of Besifloxacin, Gatifloxacin, and Moxifloxacin in Human Conjunctiva After Topical Instillation

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

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
119 (actual)
Sponsor
Bausch & Lomb Incorporated · Industry
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

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.

Conditions

Interventions

TypeNameDescription
DRUGGatifloxacinGatifloxacin 0.3% one drop instilled into study eye at visit 2.
DRUGMoxifloxacinMoxifloxacin 0.5% one drop instilled into study eye at visit 2.
DRUGBesifloxacinBesifloxacin 0.6% one drop instilled into study eye at visit 2.

Timeline

Start date
2009-03-01
Primary completion
2009-04-01
Completion
2009-04-01
First posted
2009-05-21
Last updated
2011-12-09

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00905762. Inclusion in this directory is not an endorsement.