One Hour Preoperative Gatifloxacin

Phase 4

Completed

• Conditions: Ophthalmic Surgery
• Interventions: Drug: Zymar

• Registration Number: NCT00350363
• Lead Sponsor: Stanford University

Brief Summary

Comparison of 1 day versus 1 hour application of topical Zymar.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2006-07-05
• Study First Submitted QC: 2006-07-05
• Study First Posted: 2006-07-10
• Study Start: 2007-01
• Primary Completion: 2010-12
• Study Completion: 2010-12
• Results First Submitted: 2014-05-15
• Status Verified: 2015-01
• Results First Submitted QC: 2015-01-26
• Last Update Submitted: 2015-01-26
• Results First Posted: 2015-01-29
• Last Update Posted: 2015-01-29

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

• ophthalmic surgery

Exclusion Criteria

• taken antibiotics, allergic to fluoroquinolones

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
1 hour gatifloxacin	Zymar	presence of conjunctival bacteria 1 hour after administration of topical gatifloxacin

Primary Outcome Measures

Name	Time	Method
Number of Participant With Positive Culture	2 weeks

Trial Locations

Locations (1)

Stanford; 🇺🇸 Stanford, California, United States