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
PHASE4
INTERVENTIONAL
2006-03-31
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
SINGLE_GROUP
TREATMENT
NONE
Interventions
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The cessation of anti-aggregative treatment for 10 days
Eligibility Criteria
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Inclusion Criteria
* over 20 years old
* patients who can stop their anti-aggregative treatment for 10 days
Exclusion Criteria
* post ocular surgeries
20 Years
ALL
No
Sponsors
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Sheba Medical Center
OTHER_GOV
Principal Investigators
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Hani Levkovitch-Verbin, MD
Role: PRINCIPAL_INVESTIGATOR
Goldscheleger Eye Institute, Sheba Medical Center
Locations
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Goldschleger Eye Institute
Tel Litwinsky, , Israel
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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SHEBA-05-3876-HLV-CTIL
Identifier Type: -
Identifier Source: org_study_id
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