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
| Type | Name | Description |
|---|---|---|
| DRUG | Travoprost/timolol therapy | Evaluation of 24-hour pressure efficacy with travoprost/timolol therapy after 3 months of chronic dosing |
| DRUG | Latanoprost/Timolol therapy | Evaluation 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.