Fort Myers, Florida 33901


This study will evaluate the intraocular pressure-lowering effect and safety of Bimatoprost SR compared with selective laser trabeculoplasty in patients with open-angle glaucoma or ocular hypertension who are not adequately managed with topical IOP-lowering medication.


Inclusion Criteria: - Diagnosis of either Open-Angle Glaucoma or Ocular Hypertension in each eye that require IOP lowering treatment. Exclusion Criteria: - Eye surgery (including cataract surgery) and or eye laser surgery within the past 6 months. - Enrollment in other studies using Bimatoprost SR.



Primary Contact:

Study Director
Marina Bejanian

Clinical Trial Registry Team
Phone: 877-277-8566

Backup Contact:


Location Contact:

Fort Myers, Florida 33901
United States

Study Coordinator
Phone: 239-939-0413

Site Status: Recruiting

Data Source:

Date Processed: January 21, 2020

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