Status:

COMPLETED

A 5-Year Postmarketing Safety Study Of Xalcom In Patients With Open Angle Glaucoma Or Ocular Hypertension

Lead Sponsor:

Pfizer

Conditions:

Glaucoma, Open-Angle

Ocular Hypertension

Eligibility:

All Genders

18+ years

Phase:

PHASE3

Brief Summary

To estimate the frequency of patients with ocular/periorbital adverse events. To identify any possible long-term adverse consequences of increased iris pigmentation and to follow serious adverse event...

Eligibility Criteria

Inclusion

  • Patients with open angle glaucoma and/or ocular hypertension requiring a reduction of IOP who were insufficiently responsive to topical betablockers

Exclusion

  • Previous and current treatment with any topical ophthalmic drug containing prostaglandins; any condition in which treatment with the betablocking agent, timolol, was contraindicated.

Key Trial Info

Start Date :

February 1 2002

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

Estimated Enrollment :

976 Patients enrolled

Trial Details

Trial ID

NCT00150267

Start Date

February 1 2002

Last Update

November 5 2008

Active Locations (74)

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Page 1 of 19 (74 locations)

1

Pfizer Investigational Site

Sydney, New South Wales, Australia, 2000

2

Pfizer Investigational Site

Sydney, New South Wales, Australia, 2067

3

Pfizer Investigational Site

Antwerp, Belgium, 2020

4

Pfizer Investigational Site

Brussels, Belgium, 1090