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The Collar Post Anterior Cervical Spine Surgery Study (C-PASS)

U

Unity Health Toronto

Status

Unknown

Conditions

Cervical Myelopathy
Cervical Radiculopathy

Treatments

Device: Cervical collar

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The Anterior Cervical Discectomy and Fusion (ACDF) represents one of the most commonly performed spinal operations internationally, often in the context of symptomatic radiculopathy or myelopathy secondary to cervical degenerative disease. Approximately half of surgeons continue to prescribe a period of post-operative bracing with a cervical collar. However, there is currently no high quality evidence available to support the routine use of post-operative bracing after ACDF; further, braces are expensive and have been associated with a variety of local complications. In summary, the current lack of evidence, and lack of consensus amongst surgeons, regarding best practices in the use of post-operative bracing after ACDF, places the surgeon and the patient in a precarious position.

Our randomized trial comparing the impact of 6 weeks of post-operative bracing with a rigid cervical collar vs. no post-operative bracing, on a variety of clinical and radiological outcomes, for adult patients with cervical radiculopathy and/or myelopathy undergoing single or multi-level ACDF.

Full description

The Anterior Cervical Discectomy and Fusion (ACDF) represents one of the most commonly performed spinal operations internationally, often in the context of symptomatic radiculopathy or myelopathy secondary to cervical degenerative disease. Approximately half of surgeons continue to prescribe a period of post-operative bracing with a cervical collar. However, there is currently no high quality evidence available to support the routine use of post-operative bracing after ACDF; further, braces are expensive and have been associated with a variety of local complications. In summary, the current lack of evidence, and lack of consensus amongst surgeons, regarding best practices in the use of post-operative bracing after ACDF, places the surgeon and the patient in a precarious position.

Enrollment

244 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. between the ages of 18 and 80;
  2. presenting with cervical radiculopathy and/or myelopathy to one of the study centers;
  3. deemed appropriate by the attending surgeon involved for a one, two or three level plated ACDF or a one-level ACDF with a standalone interbody cage; and
  4. able to cooperate in the completion of all study consents, forms and documents. 5. Participants who are able to speak, read and write at an elementary school level

Exclusion criteria

  1. those with previous cervical surgery;
  2. those undergoing single or multi-level plated ACDF for a diagnosis related to malignancy, infection or trauma;
  3. those undergoing a single or multi-level plated ACDF augmented with a posterior cervical fusion or posterior cervical decompression and fusion;
  4. those undergoing a multi-level non-plated ACDF;
  5. those undergoing ACDF at greater than three levels, and;
  6. those with a pre-existent neurological or mental disorder which would preclude accurate evaluation and follow-up.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

244 participants in 2 patient groups

No post-operative bracing
No Intervention group
Description:
patients in this arm will not be prescribed a cervical collar following anterior cervical discectomy and fusion surgery
Post-operative bracing
Active Comparator group
Description:
Patients in this arm will be prescribed a cervical collar following anterior cervical discectomy and fusion surgery.
Treatment:
Device: Cervical collar

Trial contacts and locations

2

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Central trial contact

Kayee Tung

Data sourced from clinicaltrials.gov

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