Trials / Completed
CompletedNCT00645671
Loteprednol Etabonate Ophthalmic Ointment vs. Vehicle in the Treatment of Inflammation Following Cataract Surgery
A Randomized Multicenter, Double-Masked, Parallel-Group Clinical Safety and Efficacy Evaluation of Loteprednol Etabonate Ophthalmic Ointment, 0.5% Versus Vehicle for the Treatment of Inflammation Following Cataract Surgery
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 400 (actual)
- Sponsor
- Bausch & Lomb Incorporated · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
To evaluate the clinical safety and efficacy of Loteprednol Etabonate Ophthalmic Ointment, 0.5% vs. vehicle for the treatment of inflammation following cataract surgery
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | 0.5% Loteprednol Etabonate Ophthalmic Ointment | 1/2 inch ribbon four times a day for 14 days |
| DRUG | Vehicle of Loteprednol Etabonate Ophthalmic Ointment | 1/2 inch ribbon four times a day for 14 days |
Timeline
- Start date
- 2008-03-01
- Primary completion
- 2009-03-01
- Completion
- 2009-03-01
- First posted
- 2008-03-28
- Last updated
- 2015-03-24
- Results posted
- 2010-09-23
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00645671. Inclusion in this directory is not an endorsement.