Clinical Trials Directory

Trials / Completed

CompletedNCT01779284

Travoprost/Timolol vs Latanoprost/Timolol Fixed Combination Therapy

24-Hour Efficacy of Travoprost/Timolol Benzalkonium Chloride BAK Free Compared With Latanoprost/Timolol Fixed Combination Therapy in Subjects With Open-Angle Glaucoma Insufficiently Controlled With Latanoprost Monotherapy

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
42 (actual)
Sponsor
Aristotle University Of Thessaloniki · Academic / Other
Sex
All
Age
29 Years – 80 Years
Healthy volunteers
Not accepted

Summary

The primary objective of this crossover trial is to compare the 3-month, mean 24-hour intraocular pressure (IOP) control and safety obtained with two popular fixed combinations in glaucoma patients insufficiently controlled with latanoprost monotherapy. This study will compare the 24-hour efficacy of travoprost/timolol fixed combination without benzalkonium chloride given once in the evening, versus the latanoprost/timolol fixed combination given in the evening. It is assumed that travoprost/timolol fixed combination will provide better quality of 24-hour pressure control.

Conditions

Interventions

TypeNameDescription
DRUGTravoprost/timolol therapyEvaluation of 24-hour pressure efficacy with travoprost/timolol therapy after 3 months of chronic dosing
DRUGLatanoprost/Timolol therapyEvaluation of 24-hour pressure efficacy for this drug after 3 months of chronic therapy

Timeline

Start date
2012-01-01
Primary completion
2012-12-01
Completion
2013-01-01
First posted
2013-01-30
Last updated
2014-05-12

Locations

1 site across 1 country: Greece

Source: ClinicalTrials.gov record NCT01779284. Inclusion in this directory is not an endorsement.

Travoprost/Timolol vs Latanoprost/Timolol Fixed Combination Therapy (NCT01779284) · Clinical Trials Directory