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
| Type | Name | Description |
|---|---|---|
| DRUG | Travoprost/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.