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
NA
26 participants
INTERVENTIONAL
2024-04-05
2024-05-22
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NON_RANDOMIZED
PARALLEL
DIAGNOSTIC
NONE
Study Groups
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Dry eye patients
Collect clinical information and tear samples from patients with dry eye syndrome.
No interventions assigned to this group
Non-Dry eye patients
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with/without dry eye syndrome
compare tear ferning structure between dry eye and non-dry eye patients
Interventions
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with/without dry eye syndrome
compare tear ferning structure between dry eye and non-dry eye patients
Eligibility Criteria
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Inclusion Criteria
* For dry eye disease group:
* Schirmer's test results between 5 - 10 mm
* Tear Film Break Up Time less than 10 seconds
* Ocular Surface Disease Index of more than 25
Exclusion Criteria
* No evident ocular diseases such as cornea disease, cataracts, vitreous degeneration, glaucoma, and retinopathy.
* Belong to vulnerable groups(pregnancy woman, prisoner, ethical minorities, economic or educationally disadvantaged subjects, disabled individuals such as those at terminal stage of tumorigenesis, blindness, terminal ill individuals)
20 Years
65 Years
ALL
Yes
Sponsors
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Chung Shan Medical University
OTHER
Responsible Party
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David Pei-Cheng Lin
Chung Shan Medical University
Locations
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Jen-Ai Hospital
Taichung, , Taiwan
Countries
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Other Identifiers
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202400020B0
Identifier Type: -
Identifier Source: org_study_id
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