A Dose Ranging Study to Evaluate Safety and Efficacy of Bromfenac Ophthalmic Solution in Dry Eye Disease
Completed · Phase 3 · Has a placebo group
Conditions studied: Dry Eye Syndrome
In brief
A dose ranging study to evaluate safety and efficacy of bromfenac ophthalmic solution in dry eye disease.
Key facts
- Study ID
- NCT01212471
- Run by
- Bausch & Lomb Incorporated
- People needed
- 840
- Starts
- 2010-09-01
- Expected to finish
- 2011-12-01
- Last updated by the study team
- 2020-09-04
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Be of either gender and any race 18 years or older
You may not qualify if…
- Have a local or systemic disease that could interfere with the assessment of safety or efficacy or that is likely to result in early discontinuation from the study
Where it is running
- ISTA Pharmaceuticals, Inc. — Irvine, California, United States
Full record on ClinicalTrials.gov
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