A 6-week Safety & Efficacy Study of Combination Intraocular Pressure-lowering Therapy in Patients With Open-angle Glaucoma or Ocular Hypertension

Completed · Phase 2

Conditions studied: Glaucoma, Open-angle, Ocular Hypertension

In brief

To compare the intraocular pressure(IOP)-lowering efficacy of morning or evening instillations of a combination IOP-lowering therapy in patients with open-angle glaucoma or ocular hypertension.

Key facts

Study ID

NCT00051194

Run by

Alcon Research

Starts

2002-09-01

Expected to finish

2003-07-01

Last updated by the study team

2012-04-16

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

Where it is running

• Europe — Fort Worth, Texas, United States

Full record on ClinicalTrials.gov

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