Seattle
Seattle, Washington, 98104, United States
NCT Number: NCT00465803
The purpose of this study is to assess patient compliance with DuoTrav versus concomitant administration of Timolol 0.5% plus TRAVATAN in patients with open-angle glaucoma or ocular hypertension.
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Notify Me18 year and older
All sexes
Interventional
Phase 3
Seattle, Washington, 98104, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
One drop in the study eye(s) once daily at either 8 AM or 8 PM for twelve months using the Dosing Aid
Other names: DuoTrav
One drop in the study eye(s) once daily at 8 PM for twelve months using the Dosing Aid
Other names: TRAVATAN
One drop in the study eye(s) once daily at 8 AM or twelve months using the Dosing Aid
Time frame: 12 months
Patient compliance will be measured with a dosing aid that records time and date of study drug administration
Alcon Research
Industry
Compliance Study Comparing DuoTrav to TRAVATAN Plus Timolol Using the Dosing Aid
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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