Doppler Ultrasound Following Unicondylar Knee Replacement to Determine the Incidence of Postoperative DVT
NCT ID: NCT02148757
Last Updated: 2017-03-21
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
112 participants
INTERVENTIONAL
2011-06-30
2015-10-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
DIAGNOSTIC
NONE
Study Groups
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DVT
Doppler Ultrasound
Doppler Ultrasound
Interventions
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Doppler Ultrasound
Eligibility Criteria
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Inclusion Criteria
* Postoperative anticoagulation with aspirin 325 twice daily
* Regional anesthesia
* Inflatable garments worn during hospitalization
Exclusion Criteria
ALL
No
Sponsors
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Hospital for Special Surgery, New York
OTHER
Responsible Party
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Locations
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Hospital for Special Surgery
New York, New York, United States
Countries
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Other Identifiers
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IRB 10093
Identifier Type: OTHER_GRANT
Identifier Source: secondary_id
10093
Identifier Type: -
Identifier Source: org_study_id
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