24-Hour Intraocular Pressure (IOP) Control With Travoprost/Timolol Fixed Combination

Status

Completed

Phases

Phase 3

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT00331240

Enrollment

Registered

2006-05-29

Start date

2006-03-31

Completion date

2007-02-28

Last updated

2014-05-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Primary Open Angle Glaucoma, Exfoliation Syndrome

Brief summary

The purpose of this study is to compare the short-term (8 week) mean 24-hour intraocular pressure control and safety of TravTim fixed combination given once in the evening with placebo once in the morning versus TravTim given once in the morning with placebo once in the evening in patients with open-angle glaucoma.

Interventions

DRUGtravoprost/timolol fixed combination

DRUGplacebo (artificial tears)

Study design

Allocation

RANDOMIZED

Intervention model

CROSSOVER

Primary purpose

TREATMENT

Masking

DOUBLE

Eligibility

Sex/Gender

ALL

Age

29 Years to 80 Years

Healthy volunteers

Inclusion criteria

* POAG * Exfoliation syndrome

Exclusion criteria

* Advanced glaucoma

Countries

Greece

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026