Post-surgical Outcomes Measure Using the ERAS Protocol for Posterior Cervical Decompression and Fusion
NCT ID: NCT04315090
Last Updated: 2021-12-10
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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WITHDRAWN
OBSERVATIONAL
2020-10-09
2022-12-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
RETROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* Diagnosis of cervical myelopathy, cervical stenosis, cervical disc disorder, or cervical spondylolisthesis
Exclusion Criteria
* Emergent surgery
18 Years
89 Years
ALL
No
Sponsors
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Mayo Clinic
OTHER
Responsible Party
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Matthew T. Neal
Principal Investigator
Principal Investigators
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Matthew Neal, MD
Role: PRINCIPAL_INVESTIGATOR
Mayo Clinic
Countries
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Related Links
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Mayo Clinic Clinical Trials
Other Identifiers
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19-006598
Identifier Type: -
Identifier Source: org_study_id