Evaluation of the Signal to Noise Ratio at Various Retinal Layers
Completed
- Conditions
- Healthy Eyes
- Interventions
- Device: 3D OCT-1 MaestroDevice: DRI OCT Triton
- Registration Number
- NCT02982174
- Lead Sponsor
- Topcon Medical Systems, Inc.
- Brief Summary
Compare the signal to noise ratio of each device at various retinal layers.
- Detailed Description
Compare the signal to noise ratio of each device (SD OCT and SS OCT) at various retinal layers from the same group of subjects
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 15
Inclusion Criteria
- Male or female patients > 18 years old who have full legal capacity to volunteer on the date the informed consent is signed.
- Subjects who can follow the instructions by the clinical staff at the clinical site, and can attend examinations on the scheduled examination date.
- Subjects who agree to participate in the study.
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Exclusion Criteria
- History of cataract or ocular surgical procedures that render the cornea opaque or otherwise impact its ability to be imaged using the investigational device.
- Fixation problems which may prevent obtaining good quality images in either eye.
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Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description Normal Eyes 3D OCT-1 Maestro Subjects with no known ocular diseases will be imaged on the 3D OCT-1 Maestro and DRI OCT Triton Normal Eyes DRI OCT Triton Subjects with no known ocular diseases will be imaged on the 3D OCT-1 Maestro and DRI OCT Triton
- Primary Outcome Measures
Name Time Method Signal to noise ratio between SD OCT and SS OCT 5 minutes
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Topcon Medical Systems Inc.
🇺🇸Oakland, New Jersey, United States