Clinical Trials Directory

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

TypeNameDescription
DRUGtimolol maleate 0.5%
DRUGlatanoprost/timolol fixed combination
DRUGplacebo (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.