Prospective Randomized Comparison of Zymar(Gatifloxacin) and Vigamox (Moxifloxacin) in Killing Conjunctival Bacterial Flora Following a One-hour Application

Sponsor
Stanford University (Other)
Overall Status
Withdrawn
CT.gov ID
NCT00466570
Collaborator
(none)
0

Study Details

Study Description

Brief Summary

Topical ophthalmic antibiotics are common prescribed just prior to eye surgery to lower the risk of infection. Previous studies have suggested that antibiotics containing a preservative (Zymar) kill bacteria much quicker than those without a preservative (Vigamox). The purpose of this research is to compare how quickly to the two commonly prescribed antibiotics eliminate bacteria from the eye surface.

Condition or Disease Intervention/Treatment Phase
  • Drug: gatifloxacin, moxifloxacin
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
0 participants
Allocation:
Randomized
Intervention Model:
Factorial Assignment
Masking:
Single
Primary Purpose:
Prevention
Official Title:
Prospective Randomized Comparison of Zymar(Gatifloxacin) and Vigamox (Moxifloxacin) in Killing Conjunctival Bacterial Flora Following a One-hour
Study Start Date :
Apr 1, 2007

Outcome Measures

Primary Outcome Measures

  1. Antibiotic killing of conjunctival bacterial flora 1 hour after application []

Eligibility Criteria

Criteria

Ages Eligible for Study:
50 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Age- older than 50 years of age

  • Diagnosis- Cataract or had cataract surgery

Exclusion Criteria:
  • Systemic or topical antibiotic treatment within 30 days

  • Use of systemic or topical steroids

  • Active ocular infection

  • Ocular surgery in the past 6 months

  • Allergy to fluoroquinolones

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Stanford University

Investigators

  • Principal Investigator: Christopher Ta, MD, Stanford University

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Christopher Ta, Principal Investigator, Stanford University
ClinicalTrials.gov Identifier:
NCT00466570
Other Study ID Numbers:
  • 8924
First Posted:
Apr 27, 2007
Last Update Posted:
Jun 13, 2013
Last Verified:
Jun 1, 2013
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 13, 2013