Trials / Unknown
UnknownNCT01603030
Efficacy of Moxifloxacin/Prednisolone in Prevention of Post Surgery Inflammation
Efficacy of Moxifloxacin 0.5%/Prednisolone 1% Fixed Combination Compared With Individual Administration of Moxifloxacin 0.5% and Prednisolone 1% in the Prevention of Post Operative Inflammation in Patients Having Lasik Surgery
- Status
- Unknown
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 66 (estimated)
- Sponsor
- Adapt Produtos Oftalmológicos Ltda. · Industry
- Sex
- All
- Age
- 18 Years – 50 Years
- Healthy volunteers
- Not accepted
Summary
This is a Unicentric, double-blind, randomized, two-arm, parallel-group study to demonstrate the efficacy of moxifloxacin/prednisolone acetate fixed combination compared with individual administration of moxifloxacin + acetate Prednisolone Eye drops in Prevention of Post Operative Inflammation and Infection in LASIK surgery.
Detailed description
antibiotic/steroid combination compared to individuals components 15 days of treatment
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | moxifloxacin 0,5% + prednisolone 1% | 1 gtt, 4x/day, 15 days |
| DRUG | moxifloxacin/prednisolone combination | 1 gtt, 4x/day, 15 days |
Timeline
- Start date
- 2012-06-01
- Primary completion
- 2012-08-01
- Completion
- 2012-09-01
- First posted
- 2012-05-22
- Last updated
- 2012-05-22
Locations
1 site across 1 country: Brazil
Source: ClinicalTrials.gov record NCT01603030. Inclusion in this directory is not an endorsement.