drugset / Trial / NCT01448837

24-Hour Intraocular Pressure Control With Bimatoprost/Timolol Versus Latanoprost as First Choice

NCT01448837

Phase 4 Completed 37 enrolled Aristotle University Of Thessaloniki
RandomizedCrossoverSingle-blindTreatment

Summary

The primary objective of this crossover 24-hour Intraocular Pressure (IOP) trial is to compare the control obtained after 3 months of therapy with the bimatoprost/timolol fixed combination (BTFC, Ganfort) given once in the evening (20:00) versus latanoprost (Xalatan) administered once in the evening (20:00) in newly-diagnosed patients with exfoliation syndrome (XFS) and ocular hypertension, or exfoliative glaucoma (XFG) previously untreated and IOP greater than 29 mm Hg.

Timeline

Start
2010-04
Primary completion
2011-03
Completion
2011-03

Drugs

EvaluationDrugModalityDoseRoute
Comparator Bimatoprost Other / unclassified Topical
Comparator Latanoprost Small molecule Topical
Comparator Timolol Other / unclassified Topical

Indications