Correlation between a reduction of intraocular pressure and an increase of compliance with the eye drop guidance

Correlation between a reduction of intraocular pressure and an increase of compliance with the eye drop guidance - Effect of a guidance for eye drops on glaucoma treatment.

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000001180

Enrollment

Registered

2008-06-09

Start date

2008-01-01

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

glaucoma

Interventions

Period: for 3 months To do the explanation of the disease and guidance for eye drops. Period: for 3 months To do the explanation of the disease.

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1)Open-anglu glaucoma Phase I >19 mmHg, Phase II >16 mmHg, Phase III >14 mmHg. 2)Normal-tension glaucoma More than 80% of IOP at pretreatment.

Exclusion criteria

Exclusion criteria: 1)Patients have retinal diseases except optic neuropathy by glaucoma. 2)Patients who had attended other clinical trials 3 months before this IC.

Design outcomes

Primary

Measure	Time frame
The intraocular pressure at the 3 months.	—

Countries

Japan

Contacts

Public ContactSasamoto

Sanyudo Hospital dept. Ophthalmology

sasamoto@sanyudo.or.jp0238-24-3700

Outcome results

None listed

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