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

Full record on ClinicalTrials.gov

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