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Data Collection Study on Glaucoma Diagnosis Support Program

Data Collection Study on Glaucoma Diagnosis Support Program - Data Collection Study on Glaucoma Diagnosis Support Program

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000055801
Enrollment
640
Registered
2024-10-10
Start date
2024-10-10
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

glaucoma

Interventions

A smartphone-connected fundus camera is brought to approximately 20 mm in front of the eye to acquire fundus images. In this study, an iPhone 13 will be used as the smartphone.

Sponsors

Hiroshima University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. patients who are at least 18 years of age and less than 80 years of age (regardless of gender) at the time consent is obtained 2. patients whose consent to participate in this study is obtained in writing 3. patients who are deemed by the physician to have ocular fundus diseases that are desirable to be examined 4. patients who are capable of mydriasis

Exclusion criteria

Exclusion criteria: 1. Patients with a history of hypersensitivity to the pupil drug (tropicamide phenylephrine hydrochloride ophthalmic solution) 2. patients who have been judged by the principal investigator or a subinvestigator of the study to be unjustly disadvantaged by participation in the study 3. Patients whose participation in the study has been judged by the principal investigator or a subinvestigator to cause difficulty in the conduct or evaluation of this clinical study.

Design outcomes

Primary

MeasureTime frame
N/A (for data collection study)

Countries

Japan

Contacts

Public ContactKana Tokumo

Hiroshima University Hospital Ophthalmology

kanatokumo@hiroshima-u.ac.jp082-257-5246

Outcome results

None listed

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