Clinical Trials Directory

Trials / Completed

CompletedNCT01298687

Divided Dose of TRAVATAN®

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
67 (actual)
Sponsor
Alcon Research · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to compare the incremental dosing of travoprost ophthalmic solution versus once a day dosing of TRAVATAN® in lowering intraocular pressure (IOP) in patients with open-angle glaucoma (OAG) or ocular hypertension (OHT).

Conditions

Interventions

TypeNameDescription
DRUGTravoprost Ophthalmic Solution, 0.00013%Cumulative daily dose is below the travoprost ophthalmic solution, 0.004% once daily dose
DRUGTravoprost Ophthalmic Solution, 0.00033%Cumulative daily dose equals the travoprost ophthalmic solution, 0.004% once daily dose
DRUGTravoprost Ophthalmic Solution, 0.001%Cumulative daily dose is above the travoprost ophthalmic solution, 0.004% once daily dose
DRUGTravoprost Ophthalmic Solution, 0.00267%Cumulative daily dose is above the travoprost ophthalmic solution, 0.004% once daily dose
DRUGTravoprost Ophthalmic Solution, 0.004%
DRUGTravoprost VehicleInactive ingredients used as an active comparator

Timeline

Start date
2011-02-01
Primary completion
2011-04-01
Completion
2011-04-01
First posted
2011-02-18
Last updated
2017-05-05

Source: ClinicalTrials.gov record NCT01298687. Inclusion in this directory is not an endorsement.