Study of low-responder to Tafluprost ophthalmic solution and Latanoprost ophthalmic solutio

Not Applicable

• Conditions: Glaucoma Ocular Hypertension

• Registration Number: JPRN-UMIN000002717
• Lead Sponsor: Kyoto University Hospital Department of Ophthalmology and visual sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2010-01-01
• Study Completion: 2010-12-01
• Last Update Posted: 17 October 2023

Recruitment & Eligibility

• Status: Complete: follow-up complete
• Sex: All
• Target Recruitment: 100

Inclusion Criteria

Not provided

Exclusion Criteria

1) Having any hypersensitivity to test drugs. 2) Having severe visual field defect (HFA <-15dB) 3) Having absolute scotoma within 5 degrees in the center of the visual field. 4) Having any corneal abnormality or other condition preventing reliable applanation tonometry. 5) Having history of glaucoma surgery. 6) Having history of cataract surgery within 1 year. 7) Having history of refractive surgery. 8) Presence of any external ocular disease, inflammation or infection of the eye and/or eyelids. 9) Subjects need to be treated with corticosteroid during study period. 10) Pregnant subjects and subjects suspected of being pregnant 11) Subjects investigators declare ineligible for any sound medical reason

Study & Design

• Study Type: Interventional
• Study Design: Not specified