Agreement and Precision Study

Topcon

Status: Completed

Conditions: Normal Eyes; Eye Abnormalities

Treatments: Device: Pachymeter

Study type: Observational

Funder types: Industry

Identifiers

NCT06733428

THQ-THINC-2024-01

Details and patient eligibility

About

To evaluate the performance of pachymetry function

Enrollment: 108 patients

Sex: All

Ages: 22+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Provide voluntary written consent
• Age at least 22 years old
• For glaucoma group only, visual field defect and optic nerve damage consistent with glaucoma
• For cornea group only, cornea abnormality

Exclusion criteria

• Ocular condition that may affect ability to perform cornea measurements
• Have or is suspected to have ocular infection
• Unable to tolerate eye testing

Trial design

108 participants in 3 patient groups

Normal

Description:

Subjects with healthy cornea

Treatment:

Device: Pachymeter

Cornea

Description:

Subjects with abnormal cornea

Treatment:

Device: Pachymeter

Glaucoma

Description:

Subjects with glaucoma

Treatment:

Device: Pachymeter