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Assessment of the Concentrations of Besifloxacin, Moxifloxacin, or Gatifloxacin in the Aqueous Humor of Subjects

NCT00824070 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 105

Last updated 2011-12-13

Study results available
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Summary

This study is being conducted to assess the concentration of besifloxacin, moxifloxacin, or gatifloxacin in aqueous humor samples collected following topical instillation of the associated formulation in subjects undergoing cataract surgery.

Conditions

  • Cataract Extraction

Interventions

DRUG

Besifloxacin hydrochloride

Instill besifloxacin study medication in the study eye prior to making an incision for cataract extraction surgery.

DRUG

moxifloxacin hydrochloride

Instill moxifloxacin study medication in the study eye prior to making an incision for cataract extraction surgery.

DRUG

gatifloxacin

Instill gatifloxacin study medication in the study eye prior to making an incision for cataract extraction surgery.

Sponsors & Collaborators

  • Bausch & Lomb Incorporated

    lead INDUSTRY

Principal Investigators

  • Eric Donnefeld · Ophthalmic Consultants of Long Island

Study Design

Allocation
RANDOMIZED
Purpose
SCREENING
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-02-28
Primary Completion
2009-07-31
Completion
2009-08-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00824070 on ClinicalTrials.gov