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Comparison of tafluprost and latanoprost on progression of visual field loss in primary open angle glaucoma: prospective, randomized, open, multi-center study.

Not Applicable
Conditions
Glaucoma
Registration Number
JPRN-UMIN000004093
Lead Sponsor
Department of Ophthalmology, Akita Univ. School of Medicine
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
120
Inclusion Criteria

Not provided

Exclusion Criteria

1. Patients had not reliable visual field measurements (fixation loss of less than 20%, and a false-negative rate and a false-positive rate of less than 33%) 2. Any corneal abnormality or other condition preventing reliable applanation tonometry. 3. Require concomitant IOP-lowering medication or glaucoma surgery 4. Refractive error in spherical equivalent exceed -8D or +8D. 5. Patient under treatment with steroids. 6. History of cataracta surgery within 6 months before start of study. 7. History of glaucoma surgery including laser iridectomy and trabeculoplasty. 8. Presence of any active external ocular disease, inflammation or infection of the eye and/or eyelids. 9. Presence of ocular disease preventing reliable visual field measurements.

Study & Design

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