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2-Site Safety Study of Besivance Versus Vigamox Prophylactically in Routine Cataract Surgery — STB-01  

Cataract Surgery Clinical Trial

Official title:
Phase IV Study: A Prospective Two-Site Study to Evaluate the Safety and Tolerance of Besivance Versus Vigamox Prophylactically Pre and Post Operatively in Subjects Undergoing Routine Cataract Surgery

Clinical Trial Summary

The purpose of this study is to demonstrate that Besivance is equal to Vigamox in safety and tolerance when used prophylactically in subjects undergoing routine cataract surgery.

Clinical Trial Description

Subjects will be assigned to receive either Besivance or Vigamox (1:1) to be administered as 1 drop in the study eye 4 times daily starting 3 days prior to cataract surgery and continuing for 7 days post-operatively.

Sixty subjects (30 from Ophthalmology Consultants and 30 from Ophthalmology Associates) of any race and either sex, requiring cataract extraction with planned implantation of a posterior chamber intraocular lens. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01455233
Study type Interventional
Source Ophthalmology Consultants, Ltd.
Contact
Status Completed
Phase Phase 4
Start date September 2010
Completion date February 2011
View Details
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