Cataract Clinical Trial
Official title:
Pilot Study on Bioavailability of Vigamox Administered as Drops vs. as Spray
The purpose of the study is to confirm that Vigamox reaches similar aqueous concentration when administered as the commercially available eye drops or as a spray delivered from a proprietary device.
Patients scheduled for elective cataract surgery, will be randomly allocated to receive
Vigamox 4 times , 1 hour prior to surgery, either via the experimental device in a spray
form, or via the regular, commercially available bottle.
Aqueous sample will be collected and submitted to a masked laboratory for measuring Vigamox
concentration.
;
Allocation: Randomized, Endpoint Classification: Pharmacokinetics/Dynamics Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor)
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