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
| Type | Name | Description |
|---|---|---|
| DRUG | Gatifloxacin | Gatifloxacin 0.3% one drop instilled into study eye at visit 2. |
| DRUG | Moxifloxacin | Moxifloxacin 0.5% one drop instilled into study eye at visit 2. |
| DRUG | Besifloxacin | Besifloxacin 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.