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OpenTrials
Completed

NCT Number: NCT02003534

A Study of 0.15% Brimonidine Tartrate in Patients With Primary Open Angle Glaucoma and Ocular Hypertension

This study will evaluate 0.15% brimonidine tartrate in patients with primary open angle glaucoma and ocular hypertension.

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Key information

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Shanghai, China

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Diagnosis of open-angle glaucoma or ocular hypertension

Exclusion criteria

  • Used Alphagan® in previous 3 months

Treatment and study plan

0.15% Brimonidine Tartrate

Drug

0.15% Brimonidine Tartrate (Alphagan® P) 1 drop in the affected eye 3 times daily for 3 months.

Other names: Alphagan® P

Primary outcomes

  1. Change From Baseline in Intraocular Pressure (IOP) in the Study Eye

    Time frame: Baseline, Month 3

    IOP is a measurement of the fluid pressure inside the eye. A negative number change from baseline indicates a reduction in IOP (improvement), and a positive number change from baseline indicates an increase (worsening).

Sponsors and collaborators

Lead sponsor

Allergan

Industry

Registry information

Acronym: APOTUS

Important dates

Study start
2010
Primary completion
2013
Study completion
2013
First posted
Dec 6, 2013
Registry last updated
Jul 22, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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