Home-OCT; evaluation of usability of eyeMO Retinal OCT

Home-OCT; evaluation of usability of eyeMO Retinal OCT - Evaluation of usability of Home-OCT

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000046555

Enrollment

Registered

2022-01-10

Start date

2022-01-10

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 eye, corioretinal disease eye

Interventions

Taking a retinal image with Home-OCT

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients over 20 years Patients with written consent for participation in the study

Exclusion criteria

Exclusion criteria: Patients with corneal opacity that may affect OCT images Patients judged to be inappropriate as a target by the judgment of a doctor

Design outcomes

Primary

Measure	Time frame
Evaluation of usability and operability of home-OCT based on the time required to complete acquisition	—

Countries

Japan

Contacts

Public ContactShozo Sonoda

Kagoshima Sonoda eye & plastic surgery clinic Ophthalmology

sonosho0110@gmail.com099-210-5311

Outcome results

None listed

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