Post-surgical Outcomes Measure Using the ERAS Protocol for Posterior Cervical Decompression and Fusion

NCT ID: NCT04315090

Last Updated: 2021-12-10

Study Results

Results pending

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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Recruitment Status

WITHDRAWN

Study Classification

OBSERVATIONAL

Study Start Date

2020-10-09

Study Completion Date

2022-12-01

Brief Summary

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This research study is being conducted to help improve the pre-operative, intra-operative, and post-operative course for patients and enhance recovery.

Detailed Description

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Conditions

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Degenerative Spinal Arthritis Cervical Myelopathy Spinal Stenosis

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* Age 18 to 89
* Diagnosis of cervical myelopathy, cervical stenosis, cervical disc disorder, or cervical spondylolisthesis

Exclusion Criteria

* Cervical injury as the indication for surgery
* Emergent surgery
Minimum Eligible Age

18 Years

Maximum Eligible Age

89 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Mayo Clinic

OTHER

Sponsor Role lead

Responsible Party

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Matthew T. Neal

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Matthew Neal, MD

Role: PRINCIPAL_INVESTIGATOR

Mayo Clinic

Countries

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United States

Related Links

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Other Identifiers

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19-006598

Identifier Type: -

Identifier Source: org_study_id