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The retrospective clinical study on inhibitory effect of 0.1% brimonidine ophthalmic solution against the optic disc hemorrhage

The retrospective clinical study on inhibitory effect of 0.1% brimonidine ophthalmic solution against the optic disc hemorrhage - Inhibitory effect of 0.1% brimonidine ophthalmic solution against the optic disc hemorrhage

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000026406
Enrollment
40
Registered
2017-03-15
Start date
2015-12-25
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

Glaucoma

Interventions

None listed

Sponsors

Fukui-ken Saiseikai Hospital
Lead Sponsor
Shimamoto Ophthalmology Clinic (Fukui)
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)Patients being treated for more than two years. 2)Patients administered with additional brimonidine for more than one year. 3)Patients with optic disc hemorrhage before administration of additional brimonidine. 4)Patients who had no addition or change with glaucoma therapeutic drugs except for addition of brimonidine addition and the end date of observation period. (If both eyes constitute indication, worse eye is chosen.)

Exclusion criteria

Exclusion criteria: 1)Patients with retinal disease. 2)Patients with corneal opacity. 3)Patients who underwent LASIK surgery. 4)Patients that cannot be enforced with accurate visual field tests. 5)Patients with MD value -25dB or below.

Design outcomes

Primary

MeasureTime frame
Comparison with the frequency of DH before and after addition of 0.1% brimonidine.

Secondary

MeasureTime frame
1) Ratio of frequency of DH occurrence 2) Intraocular pressure with Goldmann applanation tonometer

Countries

Japan

Contacts

Public ContactKoji Nitta

Fukui-ken Saiseikai Hospital Ophthalmology

nitta.koji7001@fukui.saiseikai.or.jp0776-23-1111

Outcome results

None listed

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