Clinical Trials Directory

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

TypeNameDescription
DRUGmoxifloxacin 0,5% + prednisolone 1%1 gtt, 4x/day, 15 days
DRUGmoxifloxacin/prednisolone combination1 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.