IOP-Lowering Efficacy of Brinzolamide 1.0% Added to Travoprost 0.004%/Timolol 0.5% Fixed Combination as Adjunctive Therapy

Uncontrolled glaucoma patients being treated with a prostaglandin agent alone or in combination with adjunctive drugs in fixed or unfixed combinations, will be switched from their current therapy to travoprost/timolol fixed combination and either Azopt or...

Date First Received: September 27, 2006

Last Updated: April 21, 2008

Verified by: Alcon Research, April 2008

Clinical Trial Phase: Phase 4 | Start Date: September 2006

Overall Status: Completed

Estimated Enrollment: 195

Brief Summary

Official Title: “IOP-Lowering Efficacy of Brinzolamide 1.0% Added to Travoprost 0.004%/Timolol 0.5% Fixed Combination as Adjunctive Therapy”

Condition Keyword(s):

Intervention(s):

Uncontrolled glaucoma patients being treated with a prostaglandin agent alone or in combination with adjunctive drugs in fixed or unfixed combinations, will be switched from their current therapy to travoprost/timolol fixed combination and either Azopt or placebo

Study Type: Interventional

Study Design: Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Efficacy Study

Study Primary Completion Date: August 2007

Intervention(s) in this Clinical Trial

  • Drug: Azopt

Outcome Measures for this Clinical Trial

Primary Measures

  • IOP lowering

Secondary Measures

  • safety

Criteria for Participation in this Clinical Trial

Inclusion Criteria:

  • Glaucoma

Exclusion Criteria:

  • Under 18

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 Sponsor Information

Lead Sponsor: Alcon Research

Overall Clinical Trial Officials and Contacts

Mark Jasek Study Director Alcon Research  

Additional Information

Information obtained from ClinicalTrials.gov on October 10, 2008

Link to the current ClinicalTrials.gov record. http://clinicaltrials.gov/show/NCT00382226

Study ID Number: CM-05-10

ClinicalTrials.gov Identifier: NCT00382226

Health Authority: Australia: Ministry of Health

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