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

NeuroSpine Center of Wisconsin

Status: Completed

Conditions: Cervical Stenosis

Treatments: Other: Enhanced recovery after surgery protocol

Study type: Observational

Funder types: Other

Identifiers

NCT07242989

TMW-2025-001

Details and patient eligibility

About

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

Enrollment: 100 patients

Sex: All

Volunteers: No Healthy Volunteers

Inclusion criteria

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

Exclusion criteria

• patients who represent an inordinate risk to undergo general anesthesia in the outpatient setting.

Trial design

100 participants in 1 patient group

Posterior Cervical Decompression, Instrumentation and Fusion Patients

Description:

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

Treatment:

Other: Enhanced recovery after surgery protocol