Assessment of the Concentrations of Besifloxacin, Moxifloxacin, or Gatifloxacin in the Aqueous Humor of Subjects
Completed · Phase 1
Conditions studied: Cataract Extraction
In brief
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.
Key facts
- Study ID
- NCT00824070
- Run by
- Bausch & Lomb Incorporated
- People needed
- 105
- Starts
- 2009-02-01
- Expected to finish
- 2009-08-01
- Last updated by the study team
- 2011-12-13
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Subjects who are a candidate for a routine, uncomplicated, primary cataract extraction.
- Subjects who, in the Investigator's opinion, have potential for postoperative best corrected Snellen visual acuity of at least 20/200 in the study eye.
You may not qualify if…
- Subjects who have a known sensitivity, contraindication, or allergy to the study medication(s) or their components.
- Subjects who had any corneal refractive surgery in the study eye.
- Subjects who have a history or presence of chronic generalized systemic disease that the Investigator feels might increase the risk to the subject or confound the result of the study.
- Subjects who had ocular surgery in the study eye, including laser procedures, within the past 6 months.
- Subjects who have taken any topical ocular medication in the study eye, other than those required by the protocol and permitted for surgery, during the 24 hours prior to the study medication being instilled.
- Subjects who use any antibiotics (e.g., systemic or topical) within the 7 days prior to the surgery date.
- Subjects who are monocular.
Where it is running
- Ophthalmic Consultants of Long Island — Rockville Centre, New York, United States
Full record on ClinicalTrials.gov
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