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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COMPLETED
108 participants
OBSERVATIONAL
2025-01-09
2025-01-28
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
Subjects with healthy cornea
Pachymeter
Measure the thickness of the cornea
Cornea
Subjects with abnormal cornea
Pachymeter
Measure the thickness of the cornea
Glaucoma
Subjects with glaucoma
Pachymeter
Measure the thickness of the cornea
Interventions
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Pachymeter
Measure the thickness of the cornea
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Age at least 22 years old
* For glaucoma group only, visual field defect and optic nerve damage consistent with glaucoma
* For cornea group only, cornea abnormality
Exclusion Criteria
* Have or is suspected to have ocular infection
* Unable to tolerate eye testing
22 Years
ALL
Yes
Sponsors
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Topcon Corporation
INDUSTRY
Responsible Party
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Locations
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Illinois College of Optometry
Chicago, Illinois, United States
Countries
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Other Identifiers
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THQ-THINC-2024-01
Identifier Type: -
Identifier Source: org_study_id
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