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Fort Worth, Texas 76134


The purpose of this study to assess the safety and IOP-lowering efficacy of changing to Duo-Travatan from prior Timolol 0.5% monotherapy in uncontrolled patients with open-angle glaucoma or ocular hypertension.


Inclusion Criteria: - Clinical diagnosis of ocular hypertension - Primary open-angle or pigment dispersion glaucoma in both eyes - IOP of between 19 to 35 mmHg (at any time of the day) in at least one eye (which would be designated as the study eye) - Wiliness to discontinue the use of all other ocular hypotensive medication(s) prior to receiving the study medication for the entire course of the study Exclusion Criteria: - Known medical history of allergy, hypersensitivity or poor tolerance to any component of Duo-Travatan® that is deemed clinically significant in the opinion of the Principal Investigator - Corneal dystrophies in either eye - Risk of visual field or visual acuity worsening as a consequence of participation in the study, in the investigator's best judgment - Bronchial hyper reactivity, or severe chronic obstructive pulmonary disease that would preclude the safe administration of a topical beta-blocker - History of severe allergic rhinitis - A condition, which in the opinion of the Principal Investigator, would interfere with optimal participation in the study, or which would present a special risk to the subject - Participation in any other investigational study within 30 days prior to the Screening Visit



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Fort Worth, Texas 76134
United States

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Site Status: N/A

Data Source: ClinicalTrials.gov

Date Processed: August 31, 2019

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