Willing and Able Subjects for Ocular Imaging
Conditions
Brief summary
Evaluate the clinical information obtained from the use of the machines.
Detailed description
Evaluate the clinical information provided by these devices and determine their clinical utility and efficacy and safety.
Interventions
DEVICE3D OCT-1
Spectral Domain OCT Device
DEVICE3D OCT-2000
Spectral Domain OCT Device
DEVICEDRI OCT-1
Swept Source OCT Device
DEVICENW-300
Fundus Camera
DEVICECT-1P
Tonometry
DEVICETRK-2P
Tonometry, Corneal Topography
DEVICESP-1P
Specular Microscopy
DEVICESL-D701
Slit Lamp Imaging
DEVICEMC-4S
Visual Acuity Testing
Sponsors
Topcon Medical Systems, Inc.
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
Yes
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.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Device Evaluation | 1 Hour | Determine Clinical Utility, Efficacy, and Safety |
Countries
United States
Outcome results
None listed