Time course of conjuctival hyperemia induced by eybelis ophthalmic solution 0.002%

Time course of conjuctival hyperemia induced by eybelis ophthalmic solution 0.002% - Time course of conjuctival hyperemia induced by eybelis ophthalmic solution 0.002%

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000034978

Enrollment

Registered

2018-11-23

Start date

2018-11-28

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

Healthy subjects and patients with glaucoma

Interventions

Healthy subjects and patients with glaucoma

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Healthy subjects with no ocular disease and no ocular surgery. Primary open angle glaucoma patients without lens extraction.

Exclusion criteria

Exclusion criteria: Except for participants with inclusion criteria and female with pregnant.

Design outcomes

Primary

Measure	Time frame
Time course of conjuctival hyperemia and the ocular side effects indued by eybelis ophthalmic solution.	—

Secondary

Measure	Time frame
Intraocular pressure	—

Countries

Japan

Contacts

Public ContactNakakura Shunsuke

Tsukazaki Hospital Ophthalmology

shunsukenakakura@yahoo.co.jp0792728555

Outcome results

None listed

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