Safety and Efficacy Study of Brimonidine/Timolol Fixed Combination in Patients With Glaucoma or Ocular Hypertension
The purpose of this study is to assess the safety and efficacy of Brimonidine/Timolol Fixed Combination in patients with glaucoma or ocular...
Brief Summary
The purpose of this study is to assess the safety and efficacy of Brimonidine/Timolol Fixed Combination in patients with glaucoma or ocular hypertension
- Study Type: Interventional
- Study Design: Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind, Primary Purpose: Treatment
- Study Primary Completion Date: August 1999
Intervention(s) in this Clinical Trial
- Drug: brimonidine/timolol fixed combination
Outcome Measures for this Clinical Trial
Primary Measures
- IOP
Criteria for Participation in this Clinical Trial
Inclusion Criteria:
- Clinical diagnosis of glaucoma or ocular hypertension in both eyes
- Patient requires IOP-lowering in both eyes
Exclusion Criteria:
- Uncontrolled medical conditions
- Contraindication to beta-andrenoceptor antagonist or brimonidine therapy
Gender Eligibility for this Clinical Trial: Both
Minimum Age for this Clinical Trial: 21 Years
Maximum Age for this Clinical Trial: N/A
Are Healthy Volunteers Accepted for this Clinical Trial?: No
Clinical Trial Investigator Information
Lead Investigator: Allergan Industry
Additional Information
Information obtained from ClinicalTrials.gov on February 12, 2012
Link to the current ClinicalTrials.gov record. http://clinicaltrials.gov/show/NCT00332345
Study ID Number: 190342-011T
ClinicalTrials.gov Identifier: NCT00332345
Health Authority: United States: Food and Drug Administration
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The URL of this page is:
http://clinicaltrialsfeeds.org/clinical-trials/show/NCT00332345
