Outpatient Posterior Cervical Fusion: Outcomes of the First 100 Consecutive Cases

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

COMPLETED

Total Enrollment

100 participants

Study Classification

OBSERVATIONAL

Study Start Date

2019-12-10

Study Completion Date

2025-02-28

Brief Summary

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Observational study regarding outcomes, complications, and patient acceptance for 100 consecutive patients undergoing outpatient posterior cervical decompression, instrumentation and fusion.

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Detailed Description

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Conditions

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Cervical Stenosis

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Posterior Cervical Decompression, Instrumentation and Fusion Patients

100 consecutive patients with documented cervical spinal cord and/or nerve root compression unresponsive to conservative management.

Enhanced recovery after surgery protocol

Intervention Type OTHER

This is the only study evaluating OUTPATIENT posterior cervical decompression, instrumentation, and fusion patients in a prospective fashion with a median follow-up of 2.5 years.

Interventions

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Enhanced recovery after surgery protocol

This is the only study evaluating OUTPATIENT posterior cervical decompression, instrumentation, and fusion patients in a prospective fashion with a median follow-up of 2.5 years.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* patients with neurological signs and symptoms related to cervical stenosis, confirmed by MRI, who have failed to improve with appropriate conservative management.