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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TERMINATED
1500 participants
OBSERVATIONAL
2021-05-01
2023-03-01
Brief Summary
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Detailed Description
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Primary outcome:
\- The investiigators will be looking into persistent abnormal neuropathic symptoms lasting more than 7 days following a sciatic popliteal nerve block.
Conditions
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Study Design
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CASE_CONTROL
RETROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* ambulatory ankle surgery
* use of spinal Anesthesia
* use of pre-spinal anesthesia nerve block techniques
* use of sciatic nerve block
Exclusion Criteria
ALL
Yes
Sponsors
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Hospital for Special Surgery, New York
OTHER
Responsible Party
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Principal Investigators
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Sang Kim, MD
Role: PRINCIPAL_INVESTIGATOR
Hospital for Special Surgery, New York
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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2019-1642
Identifier Type: -
Identifier Source: org_study_id
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