Safety and Intraocular Pressure (IOP) Lowering Efficacy of Low Dose Travoprost
Completed · Phase 2
Conditions studied: Open-angle Glaucoma, Ocular Hypertension
In brief
The purpose of this study is to compare the safety and IOP-lowering efficacy of various low dose travoprost formulations in patients with open-angle glaucoma or ocular hypertension.
Key facts
- Study ID
- NCT00637130
- Run by
- Alcon Research
- People needed
- 138
- Starts
- 2007-10-01
- Last updated by the study team
- 2012-12-06
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients 18 years of age or older, either sex or race with open-angle glaucoma or confirmed ocular hypertension
- Other protocol-defined inclusion criteria may apply
You may not qualify if…
- Age related
- Other protocol-defined exclusion criteria may apply
Where it is running
- Contact Alcon Call Center at 1-888-451-3937 — Fort Worth, Texas, United States
Full record on ClinicalTrials.gov
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