Clinical Trials Directory

Trials / Completed

CompletedNCT01510145

Efficacy of Changing to TRAVATAN® From Prior Therapy

Multi-Center Study Comparing Efficacy and Tolerability of TRAVATAN® BAK-free (0.004% Travoprost) in Patients Previously on Latanoprost Ophthalmic Solution 0.005% Monotherapy

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
191 (actual)
Sponsor
Alcon Research · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study was to assess the efficacy and tolerability of TRAVATAN® solution without BAK (benzalkonium chloride) after changing from prior latanoprost 0.005% ophthalmic solution monotherapy in subjects with open-angle glaucoma or ocular hypertension due to tolerability issues.

Conditions

Interventions

TypeNameDescription
DRUGTravoprost 0.004% BAK-freeContaining Polyquad (PQ) preservative

Timeline

Start date
2012-02-01
Primary completion
2013-05-01
Completion
2013-05-01
First posted
2012-01-13
Last updated
2014-06-13
Results posted
2014-06-13

Source: ClinicalTrials.gov record NCT01510145. Inclusion in this directory is not an endorsement.