Clinical Trials Directory

Trials / Completed

CompletedNCT00757835

24-hr IOP With Travoprost/Timolol Compared With Latanoprost/Timolol in XFG

24-hour IOP Control With the Travoprost/Timolol Fixed Combination Compared With the Latanoprost/Timolol Fixed Combination, When Both Are Dosed in the Evening in Patients With Exfoliative Glaucoma

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
40 (actual)
Sponsor
Aristotle University Of Thessaloniki · Academic / Other
Sex
All
Age
21 Years – 85 Years
Healthy volunteers
Not accepted

Summary

A crossover, randomized, single-masked study which compares the short-term (3 months) 24-hour IOP control and safety of travoprost/timolol fixed combination given once in the evening, versus that of latanoprost/timolol fixed combination given once in the evening in patients with exfoliative glaucoma. The primary objective of this trial is to compare the quality of 24-hour IOP control after 3 months of chronic therapy with these two medications.

Conditions

Interventions

TypeNameDescription
DRUGtreatment with latanoprost/timolol fixed combinationdosing in the evening with the two fixed combinations
DRUGlatanoprost/timolol fixed combination dropsonce in the evening

Timeline

Start date
2008-05-01
Primary completion
2009-03-01
Completion
2009-03-01
First posted
2008-09-23
Last updated
2020-12-17

Source: ClinicalTrials.gov record NCT00757835. Inclusion in this directory is not an endorsement.