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The Norwegian Cervical Arthroplasty Trial

Treatment of Cervical Radiculopathy With Arthroplasty Compared With Discectomy With Fusion and Cage (ACDF. Clinical, Radiological and Biomechanical Aspects. A Randomized Multicenter Study.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00735176
Acronym
NORCAT
Enrollment
136
Registered
2008-08-14
Start date
2008-09-30
Completion date
2017-08-31
Last updated
2019-01-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Radiculopathy, Cervical

Keywords

Radiculopathy, cervical, Nerve Root Compression, Disc, intervertebral, Intervertebral Disk Displacement, Spondylosis, Spinal Osteophytosis, Arthroplasty, replacement, Diskectomy, Spinal Fusion

Brief summary

The study will compare cervical arthroplasty with cervical discectomy and fusion, in the treatment of cervical radiculopathy. The 0-hypothesis is that there is no difference between the two methods, when comparing primary and secondary outcome variables.

Detailed description

Anterior discectomy and fusion (ACDF) is in Norway currently the most common operative method against cervical radiculopathy, caused by disc herniation and/or spondylosis. In the last decade cervical arthroplasty has emerged as a new alternative operative method. Arthroplasty is claimed to preserve the natural motion of the spine, thereby preventing adjacent level disc disease and providing better clinical results. However, this hypothesis has not yet been adequately proven. In our study, we will prove if there is any real difference in terms of clinical effect between cervical arthroplasty and ACDF.We will also compare the overall costs of the two methods, including cost-utility analyses. Moreover, we will study the development of adjacent level disease by use of MRI scans, and analyze cervical spine motion and disc height by use of Distortion Compensated Roentgen Analysis (DCRA).

Interventions

Anterior cervical discectomy, followed by insertion of the Discover™ Artificial Cervical Disc

Anterior cervical discectomy and decompression, followed by insertion of a PEEK cage, which induces fusion.

Sponsors

Rikshospitalet University Hospital
CollaboratorOTHER
Haukeland University Hospital
CollaboratorOTHER
Ullevaal University Hospital
CollaboratorOTHER
University Hospital of North Norway
CollaboratorOTHER
St. Olavs Hospital
CollaboratorOTHER
Norwegian University of Science and Technology
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
25 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Age 25 - 60 years * Clinical C6 or C7 root radiculopathy with corresponding radiologic findings with or without neurological symptoms * Mechanical provoked pain which aggravate with physical activity or positive Spurling test * Radiological nerve root compression on the basis of disc herniation or spondylosis * NDI =/\> 30 percent * The patient has not responded to non-operative treatment and shown no sign of improvement during the last 6 weeks

Exclusion criteria

* Significant spondylosis involving more than one level * Intramedullary changes on MRI * Ankylosis at adjacent level * Clinical suspicion of myelopathy * Chronic generalised pain syndrome * Infection * Active cancer * Rheumatoid arthritis involving the cervical spine * Previous trauma involving the cervical spine * Pregnancy * Allergy against contents in cage/artificial disc * Previous neck surgery * Psychological or somatic illness that causes the patient not to be suitable for the study * The patient does not understand Norwegian orally or in writing. * Abuse of medication/narcotics

Design outcomes

Primary

MeasureTime frame
change in Neck Disability Index (NDI)up to 5 years

Secondary

MeasureTime frame
Clinical effect, measured by use of EQ5-D, SF-36, numeric arm/neck pain registration, dysphagia score, rate of complications/reoperations/morbidityPreoperatively. Postoperatively: 6 weeks, 3 months, 6 months, 1 year, 2 years, 5 years
Health economical aspects, measuring hospital costs, patient costs, primary health service costs, and performing cost-utility analyses.Postoperatively: 3 months, 6 months, 1 year, 2 years
Adjacent level disc disease, measured by use of MRI scans.Maximum 4 months preoperatively. Postoperatively:1 year, 2 years, 5 years
Preservation of cervical translational and rotational segmental motion, disc height and dorsoventral displacement, by use of functional X-rays with Distortion Compensated Roentgen Analysis (DCRA)Preoperatively. Postoperatively: 1 day, 6 weeks, 1 year, 2 years, 5 years

Countries

Norway

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 14, 2026