Clinical trial
24-hour Intraocular Pressure (IOP) Control With the Bimatoprost/Timolol Fixed…
NCT00486486 · Aristotle University Of Thessaloniki, Other · Completed
Key facts
| NCT number | NCT00486486 |
|---|---|
| Title | 24-hour Intraocular Pressure (IOP) Control With the Bimatoprost/Timolol Fixed Combination |
| Official title | A 3-month, 4-centre, Crossover, Double-masked Study Investigating the 24-hour Intraocular Pressure Control With the Bimatoprost/Timolol Fixed Combination Dosed Morning, or Evening in Subjects With Exfoliative Glaucoma |
| Acronym | BTFC |
| Lead sponsor | Aristotle University Of Thessaloniki, Other |
| Status | Completed |
| Phase | Phase 4 |
| Study type | Interventional |
| Conditions | Glaucoma |
| Intervention type | Drug |
| Interventions | Drug: bimatoprost/timolol fixed combination AM, Bimatoprost/timolol fixed combination dosed PM |
| Enrollment | 60 |
| Start date | Mar 1, 2007 |
| Primary completion | May 1, 2008 |
| Completion | Jul 1, 2008 |
| First posted | Jun 14, 2007 |
| Last update posted | May 12, 2014 |
| Countries | Greece |
At a glance
- 1–9 Study sites
- No Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: