A Long-term Safety Study of Once-daily Travatan

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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

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