drugset / Trial / NCT00486486
24-hour Intraocular Pressure (IOP) Control With the Bimatoprost/Timolol Fixed Combination
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | bimatoprost/timolol | Unknown | — | — |