Comparative Study of Psychology and Glaucoma Knowledge in Glaucoma Day-ward Patients Inpatients
NCT ID: NCT03125850
Last Updated: 2020-07-23
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
240 participants
INTERVENTIONAL
2017-08-10
2018-01-10
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
HEALTH_SERVICES_RESEARCH
NONE
Study Groups
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day-ward group
randomized to day ward
Participants will be randomized to day-ward group, and will accept routine treatment, care, centralized education of glaucoma knowledge
inpatient group
randomized to inpaitent
Participants will be randomized to day-ward group, and will accept routine treatment, care, centralized education of glaucoma knowledge
Interventions
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randomized to day ward
Participants will be randomized to day-ward group, and will accept routine treatment, care, centralized education of glaucoma knowledge
randomized to inpaitent
Participants will be randomized to day-ward group, and will accept routine treatment, care, centralized education of glaucoma knowledge
Eligibility Criteria
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Inclusion Criteria
2. Will receive glaucoma surgery;
3. Voluntary participation in this study;
4. Have enough language comprehension ability;
5. Best corrected visual acuity reach 0.1 or better;
6. Patient or his legal representative has sign the informed consent.
Exclusion Criteria
2. There are important viscera function failure or other serious disease, including clinical related coronary artery disease, cardiovascular disease or myocardial infarction into the group of the first six months; serious neurological or psychiatric illness; serious infections; coagulant function abnormality; general active infectious diseases; malignant tumor; serious immune diseases;
3. Patient with monocular blindness;
4. Axial length≤20 mm;
5. With other serious eye diseases;
6. Neurologic diseases that could affect the visual field;
7. 3 months prior to research to participate in any clinical study;
8. Researchers think not suitable to participate in this clinical trial subjects;
9. Refused to sign the informed consent.
12 Years
ALL
No
Sponsors
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Zhongshan Ophthalmic Center, Sun Yat-sen University
OTHER
Responsible Party
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Mingkai Lin
chief physician
Principal Investigators
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Mingkai Lin, MD
Role: STUDY_CHAIR
Zhongshan Ophthalmic Center, Sun Yat-San University
Locations
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Zhongshan Ophthalmic Center, Sun Yat-San Univerdity
Guangzhou, Guangdong, China
Countries
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Other Identifiers
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Zhongshan OC
Identifier Type: -
Identifier Source: org_study_id
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