Topical Antibiotics and Intravitreous Injections

Evaluation of efficacy of topical preoperative antibiotics in patients undergoing intravitreous injections.

Completed

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Key information

Conditions

Intravitreous Injections

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

intravitreous injection

Exclusion criteria

antibiotic use

Treatment and study plan

Gatifloxacin

Drug

Primary outcomes

Positive Culture

Time frame: Study day 1, assessed following administration of study treatment

The percentage of patients with a positive bacterial culture following administration of study treatment is presented.

Sponsors and collaborators

Lead sponsor

Stanford University

Other

Registry information

Important dates

Study start: 2008
Primary completion: 2009
Study completion: 2009
First posted: Dec 13, 2006
Registry last updated: Nov 6, 2017

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