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
700 participants
OBSERVATIONAL
2008-01-31
2013-01-31
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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primary open-angle glaucoma
No interventions assigned to this group
ocular hypertension patients
No interventions assigned to this group
normal controls
No interventions assigned to this group
Exfoliation patients
patients with exfoliation syndrome or exfoliative glaucoma
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Intraocular pressure below 21 mm Hg without glaucomatous damage
* Intraocular pressure above 21 mm Hg without glaucomatous damage
* Raised intraocular pressure with glaucomatous damage
Exclusion Criteria
* History of trauma
* Evidence of corneal abnormality that may influence IOP
* Contact lens use
* Corneal surgery
25 Years
89 Years
ALL
Yes
Sponsors
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Aristotle University Of Thessaloniki
OTHER
Responsible Party
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AGP Konstas
Professor in Ophthalmology
Principal Investigators
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Kostantinos Kaltsos, MD, PhD
Role: STUDY_DIRECTOR
1st University Dept of Ophthalmology
Locations
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Glaucoma Unit, 1st University Department of Ophthalmology
Thessaloniki, , Greece
Countries
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Other Identifiers
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A3502
Identifier Type: -
Identifier Source: org_study_id
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