drugset / Trial / NCT00486486

24-hour Intraocular Pressure (IOP) Control With the Bimatoprost/Timolol Fixed Combination

NCT00486486 ↗

Phase 4 Completed 60 enrolled Aristotle University Of Thessaloniki
RandomizedCrossoverSingle-blindTreatment

Summary

The objective of this crossover, randomized, placebo controlled, double-masked study is to compare the short-term (12 weeks) mean 24-hour IOP control and safety of the new fixed combination (bimatoprost/timolol, BTFC) given PM with placebo once in the morning, versus BTFC given AM with placebo once in the evening versus bimatoprost given in the evening in patients with exfoliative glaucoma (XFG).

Timeline

Start
2007-03
Primary completion
2008-05
Completion
2008-07

Drugs

EvaluationDrugModalityDoseRoute
Comparator bimatoprost/timolol Unknown — —

Indications