One Hour Preoperative Gatifloxacin

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

Completed

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Key information

Conditions

Ophthalmic Surgery

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Stanford

Stanford, California, 94304, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

ophthalmic surgery

Exclusion criteria

taken antibiotics, allergic to fluoroquinolones

Treatment and study plan

Zymar

Drug

zymar qid

Other names: gatifloxacin

Primary outcomes

Number of Participant With Positive Culture

Time frame: 2 weeks

Sponsors and collaborators

Lead sponsor

Stanford University

Other

Registry information

Important dates

Study start: 2007
Primary completion: 2010
Study completion: 2010
First posted: Jul 10, 2006
Registry last updated: Jan 29, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.

Completed