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Multi-Center Study Assessing the Efficacy and Tolerability of TRAVATAN® Solution Without BAK, Containing Polyquad® Preservative (0.004% Travoprost) in Patients Previously on Latanoprost 0.005% or Bimatoprost 0.01% Ophthalmic Solution Monotherapy
The purpose of this study was to assess the efficacy and tolerability of TRAVATAN® Solution without benzalkonium chloride (BAK) in patients previously on latanoprost 0.005% or bimatoprost 0.01% ophthalmic solution monotherapy.
Details
| Lead sponsor | Alcon Research |
|---|---|
| Phase | Phase 4 |
| Status | COMPLETED |
| Enrolment | 202 |
| Start date | 2011-12 |
| Completion | 2013-02 |
Conditions
- Open-Angle Glaucoma
- Ocular Hypertension
Interventions
- Travoprost 0.004%
Primary outcomes
- Mean Change in Intraocular Pressure (IOP) at 12 Weeks From Prior Therapy (Baseline) — Baseline, Week 12
IOP (fluid pressure inside the eye) was measured by Goldmann applanation tonometry. A higher IOP can be a greater risk for developing glaucoma or glaucoma progression (leading to optic nerve damage). A more negative change indicates a greater amount of improvement. One eye was chosen as the study eye, and only data from the study eye were used for the efficacy analysis.