Safety and Efficacy of Brimonidine in Patients With Glaucoma or Ocular Hypertension

This Study will evaluate the safety and efficacy of brimonidine in patients with glaucoma or ocular...

Date First Received: September 12, 2005

Last Updated: April 1, 2008

Verified by: Allergan, April 2008

Clinical Trial Phase: Phase 3 | Start Date: 

Overall Status: Completed

Estimated Enrollment: 150

Brief Summary

Condition Keyword(s):

Intervention(s):

This Study will evaluate the safety and efficacy of brimonidine in patients with glaucoma or ocular hypertension

Study Type: Interventional

Study Design: Treatment, Randomized, Double-Blind, Active Control, Parallel Assignment, Safety/Efficacy Study

Intervention(s) in this Clinical Trial

  • Drug: brimonidine

Outcome Measures for this Clinical Trial

Primary Measures

  • lowering of intraocular pressure

Criteria for Participation in this Clinical Trial

Inclusion Criteria:

  • ocular hypertension or glaucoma in both eyes
  • currently treated with brimonidine
  • requires IOP-lowering therapy in both eyes

Exclusion Criteria:

  • uncontrolled systemic disease
  • known allergy or sensitivity to brimonidine

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: Allergan

Additional Information

Information obtained from ClinicalTrials.gov on September 05, 2008

Link to the current ClinicalTrials.gov record. http://clinicaltrials.gov/show/NCT00168363

Study ID Number: 190342-022

ClinicalTrials.gov Identifier: NCT00168363

Health Authority: United States: Food and Drug Administration

Link to Clinical Trial Results

Clinical Trials Authorship and Review

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