One Hour Preoperative Gatifloxacin - Tabular View

Tracking Information

First Received Date ^ICMJE

July 5, 2006

Last Updated Date

January 23, 2007

Start Date ^ICMJE

Primary Completion Date

Current Primary Outcome Measures ^ICMJE

Original Primary Outcome Measures ^ICMJE

Change History

Complete list of historical versions of study NCT00350363 on ClinicalTrials.gov Archive Site

Current Secondary Outcome Measures ^ICMJE

Original Secondary Outcome Measures ^ICMJE

Descriptive Information

Brief Title ^ICMJE

One Hour Preoperative Gatifloxacin

Official Title ^ICMJE

One Hour Preoperative Gatifloxacin

Brief Summary

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

Detailed Description

Study Phase

Phase IV

Study Type ^ICMJE

Interventional

Study Design ^ICMJE

Non-Randomized, Single Blind, Dose Comparison, Parallel Assignment

Condition ^ICMJE

Ophthalmic Surgery

Intervention ^ICMJE

Drug: Zymar

Study Arms / Comparison Groups

Publications *

* Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.

Recruitment Information

Recruitment Status ^ICMJE

Recruiting

Enrollment ^ICMJE

Completion Date

Primary Completion Date

Eligibility Criteria ^ICMJE

Inclusion Criteria:

ophthalmic surgery

Exclusion Criteria:

taken antibiotics, allergic to fluoroquinolones

Gender

Both

Ages

18 Years and older

Accepts Healthy Volunteers

Contacts ^ICMJE

Contact: Christopher Ta, MD

650-725-6995

Location Countries ^ICMJE

United States

Administrative Information

NCT ID ^ICMJE

NCT00350363

Responsible Party

Study ID Numbers ^ICMJE

5004

Study Sponsor ^ICMJE

Stanford University

Collaborators ^ICMJE

Investigators ^ICMJE

Principal Investigator:

Christopher Ta, MD

Stanford University

Information Provided By

Stanford University

Verification Date

January 2007

^ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP