NCT00486486View on ClinicalTrials.gov

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

PHASE4CompletedINTERVENTIONAL
Enrollment

60

Participants

Timeline

Start Date

March 31, 2007

Primary Completion Date

May 31, 2008

Study Completion Date

July 31, 2008

Conditions
Glaucoma
Interventions
DRUG

Drug: bimatoprost/timolol fixed combination AM

3-month chronic dosing in the morning

DRUG

Bimatoprost/timolol fixed combination dosed PM

Evening dosing of bimatoprost/timolol fixed combination for a period of 3 months

Trial Locations (2)

546 36

Glaucoma Unit, 1st University Department of Ophthalmology, Thessaloniki

Unknown

Glaucoma Unit, 1st University Dept of Ophthalmology, Thessaloniki

All Listed Sponsors
lead

Aristotle University Of Thessaloniki

OTHER

NCT00486486 - 24-hour Intraocular Pressure (IOP) Control With the Bimatoprost/Timolol Fixed Combination | Biotech Hunter | Biotech Hunter