Impact of Peripheral Nerve Blockade on Outcomes After Total Knee Replacement
NCT ID: NCT02742961
Last Updated: 2016-04-19
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
178214 participants
OBSERVATIONAL
2002-04-30
2014-03-31
Brief Summary
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Detailed Description
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The investigators will develop a non-parsimonious propensity score to control for potential indication bias and confounding in this observational study. Using the propensity score the investigators will match patients who receive a peripheral nerve block to a patient who did not to estimate the independent association of peripheral nerve blocks with our study outcomes.
Conditions
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Study Design
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COHORT
RETROSPECTIVE
Study Groups
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Peripheral nerve block
Intervention arm. Participants who receive a peripheral nerve block identified through submission of an appropriate physician billing code
Peripheral nerve block
A physician billing code for deposition of a local anesthetic solution around an anatomically defined nerve or nerve plexus
No peripheral nerve block
Control arm. Participants who do not receive a peripheral nerve block identified through lack of a submission of an appropriate physician billing code
No interventions assigned to this group
Interventions
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Peripheral nerve block
A physician billing code for deposition of a local anesthetic solution around an anatomically defined nerve or nerve plexus
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
18 Years
ALL
No
Sponsors
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Ottawa Hospital Research Institute
OTHER
Responsible Party
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Dan McIsaac
Associate Scientist
Locations
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Ottawa Hospital Research Institute
Ottawa, Ontario, Canada
Countries
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Other Identifiers
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DM1
Identifier Type: -
Identifier Source: org_study_id
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