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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UNKNOWN
60 participants
OBSERVATIONAL
2023-07-01
2023-10-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_ONLY
PROSPECTIVE
Study Groups
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Group 1
After using a non-contact tonometer to measure, the intraocular pressure is reduced by 0-10mmHg.
No interventions assigned to this group
Group 2
After using a non-contact tonometer to measure, the intraocular pressure is reduced by 10-20mmHg.
No interventions assigned to this group
Group 3
After using a non-contact tonometer to measure, the intraocular pressure is reduced over 20mmHg.
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
2. Measurements were taken before and after drainage, and all data were complete ;
3. The patient agrees and accepts the study.
Exclusion Criteria
2. Previous history of eye trauma, etc.
3. Cannot cooperate with the completion of intraocular pressure measurement and CASIA2 examination.
60 Years
ALL
No
Sponsors
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Wenzhou Medical University
OTHER
Responsible Party
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Yune Zhao
Principal Investigator
Locations
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Eye Hospital of Wenzhou Medical College
Wenzhou, Zhejiang, China
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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20230301CTR
Identifier Type: -
Identifier Source: org_study_id
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