IMOvifa Perimeter Reference Database

New View Optometric Center

Status: Completed

Conditions: Normal Eyes

Treatments: Device: Visual field

Study type: Observational

Funder types: Industry

Identifiers

NCT05792046

NVOC-2023-02

Details and patient eligibility

About

This study will collect data to establish a reference database for the IMOvifa perimeter.

Full description

This study will collect data from a reference population to be used as inputs to the calculation of age corrected significance limits for expected visual function sensitivity to establish reference limits for key output parameters for select test patterns of the IMOvifa perimeter device.

Enrollment: 376 patients

Sex: All

Ages: 22+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• 22 years of age or older on the date of informed consent
• Able to understand the written informed consent and willing to participate
• IOP ≤ 21 mmHg (each eye)
• BCVA 20/40 or better (each eye)
• Both eyes free of ocular conditions that may affect visual function (at doctor's discretion)

Exclusion criteria

• Unable to tolerate ophthalmic imaging and/or VF testing
• History of conditions known to adversely affect visual function (at doctor discretion)
• Spherical Equivalent refractive error outside the range from +6 Diopters
• Cylindrical refractive error outside the range +2.5 Diopters

Trial design

376 participants in 1 patient group

Normal

Description:

Subjects with normal visual function

Treatment:

Device: Visual field