Trials / Completed
CompletedNCT00330577
24-Hour Intraocular Pressure (IOP) And Blood Pressure Control In Glaucoma And Ocular Hypertension Patients
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 30 (planned)
- Sponsor
- Aristotle University Of Thessaloniki · Academic / Other
- Sex
- All
- Age
- 29 Years – 80 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to compare the short-term mean 24-hour intraocular pressure control, 24-hour blood pressure effect and safety of Latanoprost/Timolol fixed combination given once in the evening with placebo once in the morning versus timolol maleate 0.5% given twice daily in patients with ocular hypertension and primary open-angle glaucoma.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | timolol maleate 0.5% | |
| DRUG | latanoprost/timolol fixed combination | |
| DRUG | placebo (artificial tears) |
Timeline
- Start date
- 2006-04-01
- Primary completion
- 2007-04-01
- Completion
- 2007-07-01
- First posted
- 2006-05-29
- Last updated
- 2014-05-12
Locations
1 site across 1 country: Greece
Source: ClinicalTrials.gov record NCT00330577. Inclusion in this directory is not an endorsement.