One Hour Preoperative Gatifloxacin
Comparison of 1 day versus 1 hour application of topical Zymar...
Brief Summary
Official Title: “One Hour Preoperative Gatifloxacin”
Comparison of 1 day versus 1 hour application of topical Zymar.
- Study Type: Interventional
- Study Design: Allocation: Non-Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind
Intervention(s) in this Clinical Trial
- Drug: Zymar
Criteria for Participation in this Clinical Trial
Inclusion Criteria:
- ophthalmic surgery
Exclusion Criteria:
- taken antibiotics, allergic to fluoroquinolones
Gender Eligibility for this Clinical Trial: Both
Minimum Age for this Clinical Trial: 18 Years
Maximum Age for this Clinical Trial: N/A
Clinical Trial Investigator Information
Lead Investigator: Stanford University Other
Overall Clinical Trial Officials and Contacts
Christopher Ta, MD Principal Investigator Stanford University
Overall Contact: Christopher Ta, MD 650-725-6995
Additional Information
Information obtained from ClinicalTrials.gov on February 09, 2012
Link to the current ClinicalTrials.gov record. http://clinicaltrials.gov/show/NCT00350363
Study ID Number: 5004
ClinicalTrials.gov Identifier: NCT00350363
Health Authority: United States: Institutional Review Board
Clinical Trials content is provided directly by the U.S. National Institutes of Health via ClinicalTrials.gov and is not reviewed separately by ClinicalTrialsFeeds.org. Every page of specific clinical trials information contains a unique identifier which can be used to find further details directly from the National Institutes of Health.
The URL of this page is:
http://clinicaltrialsfeeds.org/clinical-trials/show/NCT00350363
