ClinicalTrials.Veeva

Menu

Stand-Alone Cage Verus Anterior Plating for Anterior Cervical Discectomy and Fusion.

Rush logo

Rush

Status

Withdrawn

Conditions

Degenerative Disc Disease
Cervical Spine Degeneration

Treatments

Device: Interbody Cage and Anterior Plating
Device: Interbody Cage

Study type

Interventional

Funder types

Other

Identifiers

NCT03312192
14021901

Details and patient eligibility

About

The purpose of this study is to compare the clinical results between two different techniques for ACDF: 1. Stand-alone ACDF, which means the placement of an interbody device (cage) without anterior fixation or plating; 2. ACDF with and interbody cage and anterior plating for fixation. Both of these procedures are commonly performed at Rush with unclear advantage of one procedure over the other. Both have been associated with good to excellent clinical outcomes. The devices used in this study are approved by the Food and Drug Administration (FDA).

Full description

Anterior cervical discectomy and fusion (ACDF) is one the most common procedures performed by spine surgeons. Although ACDF with autologous bone graft and anterior plating is commonly performed, this procedure may be associated with postoperative dysphagia, significant costs and adjacent segment pathology. To address these concerns, a number of surgeons have opted to utilize an interbody cage in a stand-alone fashion with good to excellent results. However, the published data is limited and currently there in no consensus among spine surgeons regarding the best technique to achieve fusion and improve clinical outcomes in patients with degenerative disc disease in the cervical spine.

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients undergoing a primary 1- to 2-level ACDF

    (a) Diagnosis: myelopathy, radiculopathy, myeloradiculopathy, stenosis, herniated nucleus pulposus, degenerative disc disease, spondylosis, osteophytic complexes, and foraminal stenosis

  • Patients able to provide informed consent

Exclusion criteria

  • Cervical spine trauma

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

0 participants in 2 patient groups

Plate and Cage
Active Comparator group
Description:
ACDF with interbody cage and anterior plating.
Treatment:
Device: Interbody Cage and Anterior Plating
Stand Alone Cage
Active Comparator group
Description:
ACDF with stand alone interbody cage without anterior plating
Treatment:
Device: Interbody Cage

Trial documents
1

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2025 Veeva Systems