Nevanac 3-Month Safety Study With QID Dosing
Completed · Phase 3
Conditions studied: Cataract
In brief
The purpose of this study is to determine the safety of Nevanac 0.1% compared to Acular LS 0.4% and Vehicle in patients treated before cataract surgery and for approximately 90 days following surgery.
Key facts
- Study ID
- NCT00332774
- Run by
- Alcon Research
- People needed
- 149
- Starts
- 2006-02-01
- Expected to finish
- 2006-12-01
- Last updated by the study team
- 2012-03-05
Who can join
Age: 10 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients of any race or sex ages 10 years or older undergoing cataract extraction with planned implantation of a posterior chamber intraocular lens.
- Other protocol-defined inclusion criteria may apply.
You may not qualify if…
- Under 10
- Other protocol-defined exclusion criteria may apply
Where it is running
- Contact Alcon for Trial Locations — Fort Worth, Texas, United States
Full record on ClinicalTrials.gov
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