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Comparable study between bimatoprost and latanoprost/timolo fixed combination in primary open angle glaucoma patients

Comparable study between bimatoprost and latanoprost/timolo fixed combination in primary open angle glaucoma patients - Comparable study between bimatoprost and latanoprost/timolo fixed combination in primary open angle glaucoma patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000004595
Enrollment
80
Registered
2010-12-01
Start date
2010-12-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Primary open angle glaucoma patients

Interventions

bimatoprost administration latanoprost/timolol fixed combination administration

Sponsors

Department of Ophthalmology, Kyoto Prefectural University of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) POAG patients 2) Under latanoprost monotherapy more than 4 weeks 3) Need to decrease IOP 4) who have judged to have a good compliance

Exclusion criteria

Exclusion criteria: 1) past history of side effects in beta blocker usage 2) any patients who have any active ocular disease except for glaucoma 3) who have any active retinal diseases 4) past history of reflactive surgery, filtering surgery, and trabeculotomy 5) any intraocular surgeries including laser therapy within 6 months 6) need contact lens usage during the study periods 7) who have the possibility to use medical therapy which influences IOP 8) who have corneal disorders which disturb the GAT measurement 9) who have decided to be inappropriate for this study by a physician in charge

Design outcomes

Primary

MeasureTime frame
intraocular pressure, ocular and general side effects—

Countries

Japan

Contacts

Public ContactKazuhiko Mori, Morio Ueno, Yoko Ikeda

Kyoto Prefectural University of Medicine Department of Ophthalmology

kmori@koto.kpu-m.ac.jp075-151-5575

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026