The purpose of this study is to describe the long-term safety of a fixed combination product
containing an alternative preservative, dosed once daily for 12 months, in patients with
open-angle glaucoma or ocular hypertension.
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Full eligibility criteria for NCT00928590
Ages eligible for Study
18 Years and older
Genders eligible for Study
Accepts Healthy Volunteers
Willing and able to sign an informed consent document.
Open-angle glaucoma or ocular hypertension who would benefit from a fixed combination medication, in the opinion of the investigator.
Stable treatment of an IOP-lowering medication.
Other protocol-defined inclusion criteria may apply.
Pregnant, breastfeeding, or not using adequate birth control.
Best-corrected visual acuity (BCVA) worse than 55 ETDRS letters.
Other protocol-defined exclusion criteria may apply.
All locations for NCT00928590
View full eligibility
Tris trial is registered with FDA with number: NCT00928590. The sponsor of the trial is Alcon Research and it is looking for 155 volunteers for the current phase.
Official trial title: A Twelve-Month Open-Label Safety Study of Polyquaternium-Preserved DuoTrav APS Dosed Once Daily in Patients With Open-Angle Glaucoma or Ocular Hypertension
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