Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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WITHDRAWN
OBSERVATIONAL
2014-07-31
2015-04-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Normal Healthy Eyes
Normal healthy eyes with no known ocular diseases
3D OCT-1
Spectral Domain OCT Device
3D OCT-2000
Spectral Domain OCT Device
DRI OCT-1
Swept Source OCT Device
NW-300
Fundus Camera
CT-1P
Tonometry
TRK-2P
Tonometry, Corneal Topography
SP-1P
Specular Microscopy
SL-D701
Slit Lamp Imaging
MC-4S
Visual Acuity Testing
Interventions
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3D OCT-1
Spectral Domain OCT Device
3D OCT-2000
Spectral Domain OCT Device
DRI OCT-1
Swept Source OCT Device
NW-300
Fundus Camera
CT-1P
Tonometry
TRK-2P
Tonometry, Corneal Topography
SP-1P
Specular Microscopy
SL-D701
Slit Lamp Imaging
MC-4S
Visual Acuity Testing
Eligibility Criteria
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Inclusion Criteria
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
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.
18 Years
80 Years
ALL
Yes
Sponsors
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Topcon Medical Systems, Inc.
INDUSTRY
Responsible Party
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Principal Investigators
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Danny Leung
Role: PRINCIPAL_INVESTIGATOR
Topcon Corporation
Locations
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Topcon Medical Systems, Inc.
Oakland, New Jersey, United States
Countries
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Other Identifiers
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Topcon-001-2014
Identifier Type: -
Identifier Source: org_study_id
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