Spinal Stenosis Clinical Trial
Official title:
Long-term Follow-up of Movement of the Cervical Spine After Anterior Cervical Discectomy (ACD) or Anterior Cervical Discectomy With Arthroplasty (ACDA)
Verified date | May 2021 |
Source | Zuyderland Medisch Centrum |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Rationale: Cervical degenerative disc disease (CDDD) is a common cause of cervical radiculopathy, myelopathy or myeloradiculopathy. Surgical treatment is indicated when conservative therapies do not provide sufficient relief or when neurological complaints are progressive. The main surgical techniques are anterior cervical discectomy with (ACDF) or without fusion (ACD), whereas both techniques result in high fusion rates. Short term outcomes of surgery show good clinical results. Long term follow-up shows a drop-in satisfaction rates, often due to the occurrence of new complaints. Pathology is often located at levels adjacent to the previously operated segment, known as adjacent segment disease (ASDis). This is thought to be the results of loss of motion at the previously operated and fused segment. Anterior cervical discectomy with arthroplasty (ACDA) is developed in an effort to reduce the incidence of ASDis by preserving physiological motion in the operated segment. Objective: To investigate physiological motion of the cervical spine the investigators will analyze motion patterns at the long-term in patients who underwent surgical treatment for CDDD, either ACD or ACDA. Study design: Fundamental research. This is a prospective study that includes a cohort of patients previously operated in the setting of a randomized controlled trial. Study population: Adult patients with an indication of surgical treatment for cervical radiculopathy as a consequence of CDDD were enrolled in an RCT between 2007 and 2014 and assigned to undergo ACD or ACDA. Flexion and extension cinematographic recordings of the cervical spine were performed, with the last one at one-year follow-up. The majority of patients in the ACDA group (80%) showed a normal sequence of segmental contribution, which was not the case in the ACD group. This cohort will now be asked to participate in the long-term follow-up study assessing the motion patterns 6-13 years after ACD or ACDA surgery. Intervention: One flexion and extension cinematographic recording of the cervical spine and will be made. Main study parameters/endpoints: The sequence of segmental contributions in sagittal rotation during flexion and extension of the cervical spine will be assessed in the long-term follow-up of surgical treatment. Secondary outcomes will be to assess the amount of degeneration based on the Kellgren Score (KS) and the segmental range of motion (sROM). Long term clinical outcomes will be assessed according to VAS, NDI, SF-36 and Odom's criteria. Patients will be asked whether they have new neurological symptoms and whether they have had a re-operation. Nature and extent of the burden and risks associated with participation, benefit and group relatedness: Participants receive cinematographic recordings once. The amount of radiation is a negligible risk. There will be no health benefits. There will be no follow-up.
Status | Completed |
Enrollment | 20 |
Est. completion date | October 25, 2022 |
Est. primary completion date | October 12, 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | N/A and older |
Eligibility | Inclusion criteria for the previous RCT were: - An indication for ACD because of a monoradicular syndrome, corresponding to the C5-C6 or C6-C7 level, with corresponding pathology on MRI. - Aged 18-55 years. - Able to actively perform flexion/extension movement. - Able to read the information form and sign IC. For this long-term follow-up study, inclusion criteria are: - All participants of previous RCT - Able to perform flexion/extension movement of the cervical spine - Signed IC. Patients were excluded in the previous RCT based on the following criteria, and will now be excluded based on the same criteria: - Ongoing or active infection. - Previous or actual tumorous processes in the cervical region. - Pregnancy. - Previous radiation therapy in the cervical region. - Not being able to speak Dutch. |
Country | Name | City | State |
---|---|---|---|
Netherlands | Zuyderland Medisch Centrum | Heerlen | Limburg |
Lead Sponsor | Collaborator |
---|---|
Zuyderland Medisch Centrum |
Netherlands,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Motion Analysis | The sequence of segmental contributions in sagittal rotation during flexion and extension in the lower cervical spine at the long-term after ACDA or ACD surgery for CDDD will be defined. There will be differentiated between normal or abnormal movement amongst ACD and ACDA. | 9,5 years average | |
Primary | Level of Degeneration | At the start of the cinematographic recording, one image will be saved as a lateral X-ray of the cervical spine to determine Kellgren's Score (KS).
The KS will be determined by two neurosurgeons and is a scoring method to determine severity of degenerative disc disease, using five gradations: Grade 0: absence of degeneration in the disc. Grade 1: minimal anterior osteophytosis. Grade 2: definite anterior osteophytosis, possible narrowing of the disc space, some sclerosis of the vertebral plates. Grade 3: moderate narrowing of the disc space, sclerosis of the vertebral plates, osteophytosis. Grade 4: severe narrowing of the disc space, severe sclerosis of the vertebral plates, multiple large osteophytes. |
9,5 years average | |
Secondary | VAS Score | Patients will be asked to indicate the VAS score for neck and arm pain (both left and right) will be asked | 9,5 years average | |
Secondary | NDI | The NDI is a modification of the Oswestry Low Back Pain Disability Index. It is a patient- completed, condition-specific functional status questionnaire with 10 items including pain, personal care, lifting, reading, headaches, concentration, work, driving, sleeping and recreation. Each section is scored on a 0 to 5 rating scale, in which zero means 'No pain' and 5 means 'Worst imaginable pain'. Al the points can be summed to a total score. The test can be interpreted as a raw score, with a maximum score of 50, or as a percentage. 0 points or 0% means: no activity limitations, 50 points or 100% means complete activity limitation. | 9,5 years average | |
Secondary | SF-36 | The SF-36 health survey will be used to assess both mental and physical health from the patient's perspective | 9,5 years average | |
Secondary | Odom's Outcome Criteria | The Odom's Outcome Criteria will be evaluated in all patients. This score was developed to assess clinical outcomes of cervical degenerative disc surgery | 9,5 years average | |
Secondary | New complaints and/or surgeries | Patients will be asked whether they have new complaints of radiculopathy, myelopathy or myeloradiculopathy and whether they underwent a re-operation for these complaints. | 9,5 years average |
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