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Evaluation of glaucoma or ocular hypertension patients with pre-existing ocular surface disease switched from a preserved prostaglandin analog – timolol fixed combination to a preservative – free latanoprost – timolol fixed combinatio

Not Applicable
Conditions
Ocular Hypertension
H40.1
Primary open-angle glaucoma
Registration Number
DRKS00024581
Lead Sponsor
Department of Ophthalmology, University hospital center Zagreb
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
30
Inclusion Criteria

•Adult (?18years) patients
•With open angle galucoma or ocular hypertension that had been controlled (stable IOP <19mmHg) by commercially available preserved PGA –timolol FC for at least 3 months
•Stable visual field (based on at least two reliable visual field tests performed within the last 12 months)
•Central corneal thickness within the range 500-580µm.
•mild to moderate hyperaemia based on MacMonnies (scores 1 and 2)

Exclusion Criteria

•Best-corrected visual acuity (BCVA) 0,1 or lower
•Severe visual field defects (MD 12 dB or higher)
•Any intraocular surgery (other than filtration surgery performed at least 6 months before screening)
•Any ocular surface abnormality preventing accurate IOP measurement
•Acute ocular inflammation
•Contact lens wearers

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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