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A Safety and Efficacy Study of Travoprost 0.004% Compared to Latanoprost 0.005% in Patients With Chronic Angle-Closure Glaucoma

This study has been completed.
Information provided by:
Alcon Research Identifier:
First received: January 3, 2003
Last updated: August 4, 2008
Last verified: August 2008
To demonstrate that the intraocular pressure(IOP)-lowering efficacy of Travoprost (0.004%) is equal or better than that of Latanoprost 0.005% in patients with chronic angle-closure glaucoma.

Condition Intervention Phase
Glaucoma, Angle-Closure
Ocular Hypertension
Drug: Travoprost (0.004%)
Drug: Latanoprost (0.005%)
Phase 3

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double-Blind
Primary Purpose: Treatment
Official Title: A Safety and Efficacy Study of Travoprost 0.004% Compared to Latanoprost 0.005% in Patients With Chronic Angle-Closure Glaucoma.

Resource links provided by NLM:

Further study details as provided by Alcon Research:

Study Start Date: January 2000
Study Completion Date: June 2003
Primary Completion Date: June 2003 (Final data collection date for primary outcome measure)

Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Adult patients of any race and either sex with chronic angle-closure glaucoma.
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Please refer to this study by its identifier: NCT00051181

United States, Texas
Fort Worth, Texas, United States
Sidney, Australia
Sponsors and Collaborators
Alcon Research
  More Information Identifier: NCT00051181     History of Changes
Other Study ID Numbers: C-01-38 
Study First Received: January 3, 2003
Last Updated: August 4, 2008
Health Authority: United States: Food and Drug Administration

Keywords provided by Alcon Research:

Additional relevant MeSH terms:
Ocular Hypertension
Glaucoma, Angle-Closure
Eye Diseases
Antihypertensive Agents processed this record on October 26, 2016