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
2017-10-03
2022-12-20
Brief Summary
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Detailed Description
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At baseline, patients will be trained to use the iCare Home tonometer, a handheld device based on rebound tonometry and designed for patients to use at home. After the training session and when patients feel confident, a measurement will be recorded. Thereafter, a new measurement will be obtained by the study staff (an optometrist or a nurse) using the same device. No IOP values will be visible for the examiner at that point. Thereafter, a single IOP measurement will be obtained by the same study staff using Goldmann applanation tonometry (GAT). Patients will then borrow the iCare Home tonometer to meaure their IOP at 06 and 10 am, and at 2, 6 and 10 pm during three consecutive days to obtain an IOP curve. Patients will come for a second visit where new measurements will be made in the same way as at baseline.
Two months after SLT, a new IOP curve will be obtained following the same procedure as pre-operatively. Patients' daily activities (diet, motion or sleeping habits) will not be controlled.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* PXG
Exclusion Criteria
* reduced hand and arm mobility (e.g. due to rheumatism)
18 Years
ALL
No
Sponsors
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St. Erik Eye Hospital
OTHER
Responsible Party
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Enping Chen
MD Ph D
Principal Investigators
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Enping Chen, MD Ph D
Role: PRINCIPAL_INVESTIGATOR
St. Erik Eye Hospital
Locations
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St Erik Eye Hospital
Stockholm, , Sweden
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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HOME SLT
Identifier Type: -
Identifier Source: org_study_id
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