Comparison of 1 day versus 1 hour application of topical Zymar.
..Date First Received: July 5, 2006
Last Updated: January 23, 2007
Verified by: Stanford University, January 2007
Clinical Trial Phase: Phase 4 | Start Date:
Overall Status: Recruiting
Brief Summary
Official Title: “One Hour Preoperative Gatifloxacin”
Condition Keyword(s):
Intervention(s):
Comparison of 1 day versus 1 hour application of topical Zymar.
Study Type: Interventional
Study Design: Non-Randomized, Single Blind, Dose Comparison, Parallel Assignment
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 Sponsor Information
Lead Sponsor: Stanford University
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 March 16, 2010
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 Authorship and Review
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