Pre-Operative Sterilization Study of Levofloxacin Ophthalmic Solution 1.5%
Not Applicable
- Conditions
- Diseases necessary for intraocular Surgery
- Registration Number
- JPRN-UMIN000007622
- Lead Sponsor
- Miyata eye Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 80
Inclusion Criteria
Not provided
Exclusion Criteria
1.Patients with history of hypersensitivity or severe adverse effects on newquinolone antibiotics 2.Patients suspecting bacterium, fungus or virus infection 3.Patients administered antibiotics or immunosuppressants within 3 months prior to the study 4.Patients hospitalized other than ocular surgeries 5.Patients with uncontrollable underlying disorders or complications 6.Pregnant or breast-feeding women 7.Patients wearing contact lenses during the study 8.Patients having history of ocular surgery within 3 months prior to the study on the study eye 9. Patients whom investigators estimate are not eligible
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pre-Operative bacterial eradication rate of Levofloxacin Ophthalmic Solution 1.5%
- Secondary Outcome Measures
Name Time Method