Trials / Completed
CompletedNCT02154217
Comparison of the Effects of Bimatoprost and a Fixed Combination of Latanoprost and Timolol on 24-hour Blood and Ocular Perfusion Pressures
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 200 (actual)
- Sponsor
- University of Milan · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This is a data revision with a focus on 24 hour perfusion pressures of data from a previous randomized, double masked, multicenter clinical trial. The aim was to compare the effect of bimatoprost and the fixed combination of latanoprost and timolol (LTFC) on 24-hour mean intraocular pressure (IOP) after patients are switched from a nonfixed combination of latanoprost and timolol. The main findings of the original trial had been published on Ophthalmology \[2007;114: 2244-2251\].
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Bimatoprost | |
| DRUG | Latanoprost/Timolol |
Timeline
- Primary completion
- 2004-12-01
- First posted
- 2014-06-03
- Last updated
- 2014-06-03
Locations
9 sites across 5 countries: Germany, Greece, Italy, Switzerland, United Kingdom
Source: ClinicalTrials.gov record NCT02154217. Inclusion in this directory is not an endorsement.