A Safety and Efficacy Study of Travoprost 0.004% Compared to Latanoprost 0.005% in Patients With Open-Angle Glaucoma (OAG) or Ocular Hypertension (OHT)
Completed · Phase 3
Conditions studied: Glaucoma, Open-Angle, Ocular Hypertension
In brief
The purpose of this study is to evaluate the safety and IOP-lowering efficacy of Travoprost (0.004%) compared to Latanoprost (0.005%) in patients with chronic open-angle glaucoma or ocular hypertension.
Key facts
- Study ID
- NCT00051142
- Run by
- Alcon Research
- Starts
- 2001-02-01
- Expected to finish
- 2004-06-01
- Last updated by the study team
- 2008-08-05
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
Where it is running
- Latin America — Fort Worth, Texas, United States
Full record on ClinicalTrials.gov
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