One Hour Preoperative Gatifloxacin
Information source: Stanford University
Information obtained from ClinicalTrials.gov on November 03, 2008
Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Ophthalmic Surgery
Intervention: Zymar (Drug)
Phase: Phase 4
Status: Recruiting
Sponsored by: Stanford University Official(s) and/or principal investigator(s):
Christopher Ta, MD, Principal Investigator, Affiliation: Stanford University
Overall contact:
Christopher Ta, MD, Phone: 650-725-6995
Summary
Comparison of 1 day versus 1 hour application of topical Zymar.
Clinical Details
Official title: One Hour Preoperative Gatifloxacin
Study design: Non-Randomized, Single Blind, Dose Comparison, Parallel Assignment
Eligibility
Minimum age: 18 Years.
Maximum age: N/A.
Gender(s): Both.
Criteria:
Inclusion Criteria:
- ophthalmic surgery
Exclusion Criteria:
- taken antibiotics, allergic to fluoroquinolones
Locations and Contacts
Christopher Ta, MD, Phone: 650-725-6995
Stanford, Stanford, California 94304, United States; Recruiting
Additional Information
Last updated: January 23, 2007
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