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NCT00332345 Clinical Trial

Safety and Efficacy Study of Brimonidine/Timolol Fixed Combination in Patients With Glaucoma or Ocular Hypertension

Ocular Hypertension Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00332345
Other study ID # 190342-011T
Secondary ID
Status Completed
Phase Phase 2
First received May 30, 2006
Last updated May 27, 2011
Start date July 1999
Est. completion date August 1999

Study information
Verified date May 2011
Source Allergan
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Interventional

Clinical Trial 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

Recruitment information / eligibility
Status Completed
Enrollment 73
Est. completion date August 1999
Est. primary completion date August 1999
Accepts healthy volunteers No
Gender Both
Age group 21 Years and older
Eligibility 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

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind, Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Drug:
• brimonidine/timolol fixed combination

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Allergan

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary IOP
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