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Clinical Trials/NCT00273455
NCT00273455
Completed
Phase 4

Lumigan Versus Cosopt

Pharmaceutical Research Network3 sites in 1 country34 target enrollmentJanuary 2006

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Open-Angle Glaucoma
Sponsor
Pharmaceutical Research Network
Enrollment
34
Locations
3
Status
Completed
Last Updated
17 years ago

Overview

Brief Summary

To compare the intraocular pressure effect and safety of the dorzolamide/timolol fixed combination given twice daily versus bimatoprost given once every evening in patients with open-angle glaucoma in patients insufficiently controlled on latanoprost monotherapy

Registry
clinicaltrials.gov
Start Date
January 2006
End Date
May 2007
Last Updated
17 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Sponsor
Pharmaceutical Research Network

Eligibility Criteria

Inclusion Criteria

  • adults with a diagnosis of bilateral open-angle glaucoma including: primary, pigment dispersion or exfoliation in both eyes
  • on no therapy the intraocular pressure should be 22-29 mm Hg inclusive at the 8:00 AM measurement
  • visual acuity should be 20/200 or better in each eye

Exclusion Criteria

  • historical failure to respond to topical beta-blockers in a clinically meaningful manner
  • any contraindication to study medications
  • any anticipated change, or modification in the 6 weeks prior to Visit 1, in systemic hypertensive therapy during the trial

Outcomes

Primary Outcomes

Not specified

Study Sites (3)

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