Trials / Completed
CompletedNCT01573910
An Evaluation of the Safety and Efficacy of Moxifloxacin Ophthalmic Solution 0.5% ((VIGAMOX®) Versus Ofloxacin Ophthalmic Solution 0.3% in the Treatment of Bacterial Conjunctivitis in Chinese Patients
An Evaluation of the Safety and Efficacy of Moxifloxacin Ophthalmic Solution 0.5% Versus Ofloxacin Ophthalmic Solution 0.3% in the Treatment of Bacterial Conjunctivitis in Chinese Patients
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 985 (actual)
- Sponsor
- Alcon Research · Industry
- Sex
- All
- Age
- 1 Year
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to evaluate Moxifloxacin 0.5% relative to Ofloxacin 0.3% in the treatment of bacterial conjunctivitis in Chinese patients.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Moxifloxacin ophthalmic solution, 0.5% | |
| DRUG | Ofloxacin ophthalmic solution, 0.3% |
Timeline
- Start date
- 2012-05-01
- Primary completion
- 2014-04-01
- Completion
- 2014-04-01
- First posted
- 2012-04-10
- Last updated
- 2015-05-12
- Results posted
- 2015-05-12
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT01573910. Inclusion in this directory is not an endorsement.