A Long-term Safety Study of Once-daily Travatan
Long term safety study of TRAVATAN in patients with Open-angle glaucoma or ocular hypertension...
Brief Summary
Official Title: “A Long-term Safety Study of Once-daily TRAVATAN”
Long term safety study of TRAVATAN in patients with Open-angle glaucoma or ocular hypertension.
- Study Type: Interventional
- Study Design: Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
- Study Primary Completion Date: March 2009
Intervention(s) in this Clinical Trial
- Drug: Travatan
- Travoprost (0.004%) 1 drop each eye once daily
Arms, Groups and Cohorts in this Clinical Trial
- Experimental: Travatan
- Travoprost (0.004%)
Outcome Measures for this Clinical Trial
Primary Measures
- Mean Intraocular Pressure
- Time Frame: At 5 years.
Safety Issue?: Yes
- Time Frame: At 5 years.
Criteria for Participation in this Clinical Trial
- Adult patients of any race and either sex with chronic angle-closure glaucoma.
Gender Eligibility for this Clinical Trial: Both
Minimum Age for this Clinical Trial: 18 Years
Maximum Age for this Clinical Trial: N/A
Are Healthy Volunteers Accepted for this Clinical Trial?: No
Clinical Trial Investigator Information
Lead Investigator: Alcon Research Industry
Additional Information
Information obtained from ClinicalTrials.gov on February 09, 2012
Link to the current ClinicalTrials.gov record. http://clinicaltrials.gov/show/NCT00051168
Study ID Number: C-02-20
ClinicalTrials.gov Identifier: NCT00051168
Health Authority: United States: Food and Drug Administration
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The URL of this page is:
http://clinicaltrialsfeeds.org/clinical-trials/show/NCT00051168
