Cervical Spondylosis Clinical Trial
— CACESOfficial title:
Economic Evaluation of Anterior Cervical Discectomy With Arthroplasty Versus Anterior Cervical Discectomy With Fusion in the Surgical Treatment of Cervical Degenerative Disc Disease, a Randomized Controlled Trial
To date, no consensus exists on which anterior surgical technique is more cost-effective to treat cervical degenerative disc disease (CDDD). The most commonly used surgical treatment for patients with single- or multilevel symptomatic CDDD is anterior cervical discectomy with fusion (ACDF). However, new complaints of radiculopathy and/or myelopathy commonly develop at adjacent levels, also known as clinical adjacent segment pathology (CASP). It remains unknown to what extent kinematics, surgery-induced fusion and natural history of disease play a role in its development. Anterior cervical discectomy with arthroplasty (ACDA) is thought to reduce the incidence of CASP by preserving motion in the operated segment. ACDA is often discouraged as the implant costs are higher whilst the clinical outcomes are similar to ACDF. However, preventing CASP might be a reason for ACDA to be a more cost-effective technique in the long-term. In this randomized controlled trial patients will be randomized to receive ACDF or ACDA in a 1:1 ratio. Adult patients with single- or multi-level CDDD and symptoms of radiculopathy and/or myelopathy will be included. The primary outcome is cost-effectiveness and cost-utility of both techniques from a societal perspective. Secondary objectives are the differences in clinical and radiological outcomes between the two techniques, as well as the qualitative process surrounding anterior decompression surgery. All outcomes will be measured at baseline and every 6 months till 4 years postoperatively. High quality evidence regarding the cost-effectiveness of both ACDA and ACDF is lacking, to date no prospective trials from a societal perspective exist. Considering the ageing of the population and the rising healthcare costs, the need for a solid clinical cost-effectiveness trial addressing this question is high.
Status | Recruiting |
Enrollment | 198 |
Est. completion date | June 1, 2028 |
Est. primary completion date | June 1, 2026 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Indication for anterior cervical decompression surgery. - Single- or multilevel CDDD between C3 and C7. - Symptoms of myelopathy, radiculopathy, or myeloradiculopathy. - In case of pure radiculopathy: refractory to at least 6 weeks of conservative therapy. - In case of myelopathy: symptomatic myelopathy. - Patients = 18 years of age. Exclusion criteria - Indication for (additional) posterior surgical approach. - Indication for additional stabilization of the pathological segment by a plate. - Previous ventral surgery of the cervical spine. - Traumatic origin of the compression. - Previous radiotherapy of the cervical spine. - Metabolic bone disease. - Inflammatory spinal disease: e.g., Bechterew's disease, Forestier's disease. - Infection of the cervical spine. |
Country | Name | City | State |
---|---|---|---|
Netherlands | Zuyderland Medical Center | Maastricht | Limburg |
Lead Sponsor | Collaborator |
---|---|
Valérie Schuermans |
Netherlands,
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* Note: There are 47 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Costs | Costs will be determined from a societal perspective.
Validated cost questionnaires for societal costs, including medical consumption, both paid and unpaid loss of productivity for patients. : Productivity Cost Questionnaire (iPCQ) for measuring productivity loss for work loss (paid and unpaid). Consists of 7 questions. the Medical Consumption Questionnaire (iMCQ) for measuring medical consumption, especially designed for the Dutch health care environment. Consists of 14 questions. Informal caregivers will be asked to fill out the Limited Valuation of Informal Care Questionnaire (iVICQ): informal care giver (ICG) productivity loss for work loss (paid and unpaid) Care-related Quality of Life instrument (CarerQol-7D). The Self-Rated Burden scale (SRB), a horizontal 'visual-analog scale' to determine the subjective burden of the caregiver on a scale from 0 (not heavy) to 10 (very heavy). |
4 years | |
Primary | Effectiveness | In the CUA, the Incremental Cost-Effectiveness Ratio (ICER) will be expressed as the incremental costs per QALY.
Quality Adjusted Life Years (QALYs) will be determined by Generic Quality of Life assessed based on the EuroQol utility scores (EQ-5D-5L). The EQ-5D-5L essentially consists of 2 pages: the EQ-5D descriptive system and the EQ visual analogue scale (EQ VAS). The descriptive system comprises five dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Each dimension has 5 levels: no problems, slight problems, moderate problems, severe problems and extreme problems. The patient is asked to indicate his/her health state by ticking the box next to the most appropriate statement in each of the five dimensions. This decision results in a 1-digit number that expresses the level selected for that dimension. The digits for the five dimensions can be combined into a 5-digit number that describes the patient's health state. |
4 years | |
Secondary | CASP | The rate of clinical adjacent segment pathology and associated additional surgeries will be assessed. | 4 years | |
Secondary | Radiological Outcomes | At 3 time points; pre-operatively, directly post-operative and one-year post-operative.
Pre-operative imaging will assess baseline degeneration according to the Kellgren-Lawrence Score, cervical sagittal alignment and baseline disc height. Moreover, a full sagittal spine X-ray will be made to assess pre-operative global balance according to the odontoid-hip axis. Post-operative: A standard cervical spine X-ray to assess the position of the implant, subsidence and cervical sagittal alignment. 1 year post-operative cervical spine X-rays will be made. A standard cervical spine X-ray will be made to assess fusion, cage subsidence, adjacent segment degeneration (KS), adjacent segment disc height and alignment. A flexion and extension X-ray will be made to assess movement. |
1 year | |
Secondary | Neck Disability Index (NDI). | 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 question is scored on a 0-5 scale, where 0 is no disability and 5 is the maximal disability possible | 4 years | |
Secondary | Visual Analogue Scale (VAS) for neck and arm pain. | Visual Analogue Scale (VAS) for neck and arm pain. Neck and arm pain are assessed separately on a horizontal 10 cm visual scale, varying from 0 cm (no pain) to 10 cm (worst pain imaginable) | 4 years | |
Secondary | Hospital Anxiety Depression Scale (HADS) | A fourteen-item scale, to determine the anxiety and depression level. Consisting of a 7-item depression scale and a 7-item anxiety scale. The score ranges from 0-21 with a high score being indicative for depression/anxiety (= 8) | 4 years | |
Secondary | modified Japanese Orthopedic Association score (mJOA) | modified Japanese Orthopedic Association score (mJOA) for myelopathy. patients. An investigator-administered tool used to evaluate neurological function in patients with cervical myelopathy. It is an 18-point scale that addresses upper (5 points) and lower extremity (7 points) motor function, sensation (3 points) and micturition (3 points). A score of 18 reflects no neurological deficits whereas a lower score indicates a greater degree of disability and functional impairment | 4 years | |
Secondary | Process Evaluation | Moreover, a process evaluation will be performed to determine the underlying values, needs, impacts and preferences of people with CDDD. The focus will be experiences and opinions of patients, caregivers, and professionals concerning the process surrounding ACDA and ACDF. A process evaluation might also identify gaps or limitations in published research with regards to important outcomes to those with lived experience. A qualitative analysis will be performed according to the framework provided by Saunders et al. | 4 years |
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