Clinical Trials Directory

Trials / Completed

CompletedNCT01493427

Efficacy of Changing to TRAVATAN® From Prior Therapy

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

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
202 (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 benzalkonium chloride (BAK) in patients previously on latanoprost 0.005% or bimatoprost 0.01% ophthalmic solution monotherapy.

Conditions

Interventions

TypeNameDescription
DRUGTravoprost 0.004%Travoprost 0.004% without benzalkonium chloride (BAK), containing Polyquad (PQ) preservative

Timeline

Start date
2011-12-01
Primary completion
2013-02-01
Completion
2013-02-01
First posted
2011-12-16
Last updated
2014-05-19
Results posted
2014-05-09

Source: ClinicalTrials.gov record NCT01493427. Inclusion in this directory is not an endorsement.