Non-Invasive Imaging of the Human Eye

Topcon

Status: Withdrawn

Conditions: Willing and Able Subjects for Ocular Imaging

Treatments: Device: CT-1P; Device: 3D OCT-1; Device: SL-D701; Device: SP-1P; Device: DRI OCT-1; Device: MC-4S; Device: NW-300; Device: 3D OCT-2000; Device: TRK-2P

Study type: Observational

Funder types: Industry

Identifiers

NCT02432898

Topcon-001-2014

Details and patient eligibility

About

Evaluate the clinical information obtained from the use of the machines.

Full description

Evaluate the clinical information provided by these devices and determine their clinical utility and efficacy and safety.

Sex: All

Ages: 18 to 80 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

1. Male or female patients from 18 to 80 years old who have full legal capacity to volunteer on the date the informed consent is signed.
2. Subjects who can follow the instructions by the clinical staff at the clinical site and can attend examinations on the scheduled examination date.

Exclusion criteria

1. History of ocular pathology.
2. History of cataract of ocular surgical procedures that render the cornea opaque or otherwise impact its ability to be imaged using the investigational device.
3. History of systemic disease
4. fixation problems which may prevent obtaining good quality images in the eye.

Trial design

0 participants in 1 patient group

Normal Healthy Eyes

Description:

Normal healthy eyes with no known ocular diseases

Treatment:

Device: CT-1P

Device: MC-4S

Device: 3D OCT-1

Device: SP-1P

Device: NW-300

Device: SL-D701

Device: 3D OCT-2000

Device: TRK-2P

Device: DRI OCT-1