Clinical Trials Directory

Trials / Completed

CompletedNCT00444184

24-hour Intraocular Pressure Control With Travoprost/Timolol Fixed Combination Versus Travoprost

A Crossover, Double-Masked Comparison Investigating the 24-Hour Intraocular Pressure Control With the Travoprost/Timolol Fixed Combination Versus Travoprost, When Both Are Given in the Evening, in Subjects With Primary Open-Angle Glaucoma

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
32 (actual)
Sponsor
Aristotle University Of Thessaloniki · Academic / Other
Sex
All
Age
29 Years – 81 Years
Healthy volunteers
Not accepted

Summary

This 8-week, crossover study will compare the quality of 24-hour IOP control with TTFC versus travoprost when both medications are dosed in the evening. Such a crossover comparison may determine the real efficacy of the new fixed combination versus travoprost monotherapy. The results should enhance the investigators understanding on the best dosing of TTFC and may influence its clinical use in Europe. Finally, the results would better delineate the future role of TTFC in glaucoma management after PG monotherapy, or instead of unfixed therapy with PG analogs and timolol. This study should assist the general ophthalmologist worldwide to plan optimal stepwise medical therapy.

Conditions

Interventions

TypeNameDescription
DRUGTravoprost/timolol fixed combination, travoprost

Timeline

Start date
2007-03-01
Primary completion
2008-01-01
Completion
2008-01-01
First posted
2007-03-07
Last updated
2014-05-12

Locations

1 site across 1 country: Greece

Source: ClinicalTrials.gov record NCT00444184. Inclusion in this directory is not an endorsement.