The Application of Enhanced Recovery After Surgery Clinical Pathway in Posterior Cervical Spine Surgery
NCT ID: NCT05149404
Last Updated: 2021-12-08
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
400 participants
OBSERVATIONAL
2020-08-01
2021-12-30
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
Study Groups
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ERAS group
No interventions assigned to this group
Conventional group
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
2. Diagnostic diagnosis of cervical spondylosis and consistent with the indications of posterior spinal canal extended laminoplasty;
3. Basis of serious diseases of centerlessness, brain, lung, kidney or other important organs, preoperative ASA score I-II;
4. Agree to participate in the study and sign the informed consent.
Exclusion Criteria
18 Years
70 Years
ALL
No
Sponsors
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Beijing Tiantan Hospital
OTHER
Beijing Chao Yang Hospital
OTHER
Peking University International Hospital
OTHER
Peking University Third Hospital
OTHER
Responsible Party
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Locations
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Peking University Third Hospital
Beijing, Beijing Municipality, China
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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LM2020289
Identifier Type: -
Identifier Source: org_study_id
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