Monoaxial vs. Polyaxial Percutaneous Hybrid Stabilization
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Monoaxial instrumentation - the M.U.S.T. Monoaxial Pedicle Screw Cannulated (Medacta International SA, Switzerland), Polyaxial instrumentation - the M.U.S.T. LT Pedicle Screw System (Medacta International SA, Switzerland).
- Who it may be relevant to
- Registry conditions: Thoracolumbar, Fractures in the Elderly. Basic parameters: from 60 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Monoaxial vs. Polyaxial Percutaneous Hybrid Stabilization for Thoracolumbar Fractures in Elderly Patients: A Randomized, Single-Blind Pilot Study
Overview
Vertebral body fractures in older adults mostly affect the thoracolumbar junction and are challenging to treat due to osteoporosis and other comorbidities. Treatment options range from conservative approaches to minimally invasive procedures like vertebroplasty or balloon kyphoplasty, as well as surgical techniques such as posterior or combined stabilization. A common method for more severe fractures (from OF3 onwards) is percutaneous bisegmental hybrid stabilization using cement-augmented pedicle screws and balloon kyphoplasty. Polyaxial screws are easier to implant but offer less biomechanical stability. In contrast, monoaxial screws provide greater stiffness, allowing better correction of kyphosis and restoration of vertebral body height. The study compares radiological and clinical outcomes in patients aged 60 and older with thoracolumbar fractures (T11-L4) between monoaxial and polyaxial hybrid stabilization. The primary goal is to evaluate and compare the degree of kyphosis correction six months after surgery.
Detailed description
Vertebral fractures in elderly patients predominantly affect the thoracolumbar spine and continue to pose a significant clinical challenge. These fractures have distinct characteristics, are increasing in incidence, and represent a major source of morbidity in this population. Patients typically present with impaired bone quality and significant comorbidities, which further complicate management. The optimal treatment of these fractures remains controversial. Treatment options range from conservative therapy and isolated vertebral body augmentation procedures - such as vertebroplasty or ballon kyphoplasty - to various posterior instrumentation techniques, and in selected cases, combined posteroanterior surgical stabilization. The choice of treatment depends not only on the specific fracture characteristics but is also influenced by the individual patient's overall condition. There is general consensus that the goals of surgical treatment include providing sufficient stability to enable early mobilization and prevent progressive deformity, achieving reduction of fracture-induced malalignment to restore sagittal alignment, decompressing neural elements in cases of neurological deficits, and ultimately maximizing clinical outcomes.
Percutaneous bisegmental hybrid stabilization is considered a standard treatment option for thoracolumbar fractures in elderly patients \[6; 7\], particularly for type 3 fractures or higher, as defined by the classification of the Spine Section of the German Society for Orthopaedics and Trauma (DGOU). This stabilization technique involves posterior cement-augmented pedicle screw instrumentation at one level above and below the fracture, combined with balloon kyphoplasty of the fractured vertebral body. While several studies have reported outcomes following combined bisegmental uncemented pedicle screw instrumentation and cement augmentation of the fractured vertebral body, specific data on percutaneous bisegmental hybrid stabilization - incorporating cement augmentation of both the pedicle screws and the fractured vertebra - remain very limited. In a retrospective study of 113 patients aged 60 years or older who underwent polyaxial percutaneous bisegmental hybrid stabilization, reported five in-patient complications (4.4%) and an average Oswestry Disability Index (ODI) score of 29.9±22.2 (range: 0-80) after a mean follow-up of 48 months (range: 24-78 months). The mean loss of reduction was 7.4°±5.6° (range: 0°-25°), with 22% of patients exhibiting a loss of ≥ 10°. Furthermore, a significant correlation was observed between the extent of reduction loss and ODI scores. In a subsequent analysis, the authors identified the superior intervertebral disc adjacent to the fractured vertebral body and the central portion of the vertebral body itself as the primary contributors to reduction loss. Notably, the relative loss of central vertebral body height was the only parameter significantly associated with the overall loss of reduction.
Hybrid stabilization has traditionally been performed using polyaxial pedicle screws, as cannulated and perforated pedicle screws designed for PMMA cement augmentation were only available in the polyaxial variant from various manufacturers. Moreover, polyaxial pedicle screws are commonly used for percutaneous instrumentation due to the ease of rod insertion. However, from a biomechanical perspective, polyaxial screws have several limitations in effective fracture stabilization, particularly when it comes to achieving and maintaining fracture reduction. In cases of a vertebral body fractures, the load-bearing capacity of the anterior column is typically compromised. In such scenarios, the ability of pedicle screw constructs to resist flexion and anterior compressive forces is critical to maintain the intraoperatively achieved fracture reduction. Monoaxial pedicle screws, when attached to a rod, form an angular-stable construct due the fixed axis between the screw head and shaft. In contrast, polyaxial screws feature a screw head that can swivel freely in multiple planes and is connected to the shaft via a coupling mechanism, potentially reducing angular stability between the screw head and shaft. Biomechanical studies have demonstrated that polyaxial screw constructs exhibit reduced stiffness compared to traditional monoaxial systems and fail at lower load levels, typically due to slippage at the screw-head interface. This polyaxial screw-head angular change may result in loss of fracture reduction and contribute to sagittal malalignment. In addition to reduced construct stiffness and the risk of postoperative reduction loss, intraoperative fracture reduction can also be challenging when using polyaxial screws for thoracolumbar fracture stabilization. With monoaxial screws, fracture reduction is typically achieved through direct screw manipulation and attachment to a lordotically pre-contoured rod. In contrast, due to the mobility of the screw heads in polyaxial systems, screw manipulation is less effective, and fracture reduction relies primarily on patient positioning. Consistent with these biomechanical considerations, several clinical studies - predominantly in younger patients - have demonstrated that overall kyphosis correction and vertebral body height restoration are significantly better following monoaxial instrumentation compared to polyaxial constructs. As a result, it has been questioned whether polyaxial instrumentation is capable of restoring anatomic sagittal alignment in the long term, or whether it should be regarded primarily as a means of preventing further collapse of the fractured vertebral body.
Taken together, hybrid stabilization using monoaxial screws may offer superior correction of fracture-induced kyphotic deformity, improved vertebral body height restoration, and reduced postoperative loss of reduction compared to hybrid stabilization with polyaxial screws.
The overall aim of this study is to compare radiological and clinical outcomes following percutaneous bisegmental hybrid stabilization using monoaxial versus polyaxial pedicle screws in patients aged 60 years or older with thoracolumbar fractures (T11-L4).
Interventions
- Device Monoaxial instrumentation - the M.U.S.T. Monoaxial Pedicle Screw Cannulated (Medacta International SA, Switzerland)
In this study, fractures between the 11th thoracic (T11) and 4th lumbar (L4) vertebra (both included) will be treated surgically using either monoaxial or polyaxial bisegmental hybrid stabilization. Hybrid stabilization consists of posterior cement-augmented pedicle screw instrumentation combined with balloon kyphoplasty of the fractured vertebral body. For bisegmental hybrid stabilization, standard cannulated and perforated pedicle screws, either monoaxial (M.U.S.T. Monoaxial Pedicle Screw Cann - Device Polyaxial instrumentation - the M.U.S.T. LT Pedicle Screw System (Medacta International SA, Switzerland)
In this study, fractures between the 11th thoracic (T11) and 4th lumbar (L4) vertebra (both included) will be treated surgically using either monoaxial or polyaxial bisegmental hybrid stabilization. Hybrid stabilization consists of posterior cement-augmented pedicle screw instrumentation combined with balloon kyphoplasty of the fractured vertebral body. For bisegmental hybrid stabilization, standard cannulated and perforated pedicle screws, either monoaxial (M.U.S.T. Monoaxial Pedicle Screw Cann
Primary outcome measures
- Overall bisegmental kyphosis correction [Time frame: 6 month]
Secondary outcome measures (12)
- Radiological outcome - Bisegmental Cobb Angle (BCA) [Time frame: 1 Year]
- Radiological outcome - Surgical bisegmental kyphosis correction (SKC) [Time frame: 1-2 weeks after post-op mobilization]
- Radiological outcome - Loss of bisegmental kyphosis correction [Time frame: 6 month]
- Radiological outcome - overall bisegmental kyphosis correction (OKC) supine [Time frame: 6 month]
- Radiological outcome - Surgical bisegmental kyphosis correction (SKC) supine [Time frame: 1-2 weeks after post-op mobilization]
- Radiological outcome - Vertebral wedge angle (VWA) [Time frame: 1 Year]
- Radiological outcome - Vertebral body height (VBH) in % [Time frame: 1 Year]
- Radiological outcome - Vertebral body compression percentage (VBCP) in % [Time frame: 1 Year]
- Radiological outcome - Disc height (DH) [mm] [Time frame: 1 Year]
- Radiological outcome - The upper disc angle (UDA) and lower disc angle (LDA) [Time frame: 1 year]
- Radiological outcome - Accuracy of pedicle screw placement [Time frame: 1 week Prior to post-op mobilization]
- Radiological outcome - cement leakage [Time frame: 1 week Prior to post-op mobilization]
Eligibility criteria
Inclusion criteria
Patient-related criteria:
- Age ≥ 60 years (male and female patients)
- Ability to understand nature, risks, and benefits of study participation and to provide written informed consent.
- Psychosocially, mentally, and physically capable of complying with all study requirements, including scheduled follow-up visits, completion of forms, and participation in all procedures as defined by the protocol.
- Ambulatory prior to fracture, with or without the use of assistive devices
Fracture-related criteria:
- Acute vertebral fractures located between T11 and L4 (inclusive)
- Fractures deemed suitable for bisegmental hybrid stabilization based on clinical and radiological assessment - primarily OF type 3 and type 4 fractures according to DGOU classification; type 2 and 5 fractures may also be included based on individual evaluation, with the final treatment decision left to the discretion of the treating surgeon.
Exclusion criteria
Patient-related criteria:
- Body mass index (BMI) > 35
- Permanent or progressive neurologic deficits (including upper motor neuron disease and myelopathy)
- Rheumatoid arthritis or known disorders of bone metabolism (excluding osteopenia/osteoporosis, Vitamin D deficiency)
- History of radiation therapy to the spine
- History of alcohol or drug abuse within the last 2 years prior to randomization
- Current therapy with high-dose systemic corticosteroids (e.g., >10 mg/day prednisone equivalent for more than 3 months)
- Ongoing or planned treatment with cytotoxic chemotherapy (excluding biologicals, immunotherapy, or targeted agents) at the time of enrollment
- Known allergy to any component of the spinal instrumentation
- Participation in other clinical investigations (drug or device) that may interfere with the outcomes of this study
Fracture-related criteria:
- Vertebral fractures associated with neurological deficits
- Fracture age > 4 weeks at the time of enrollment
- Pathological fractures due to spinal infection or metastatic bone disease
- Planned major spinal surgery within 12 months of enrollment
- Severe spinal deformities or fusion at the index or adjacent segments
- Previous spinal surgery involving the index or adjacent vertebrae, with the exception of minor non-instrumented procedures, such as simple sequestrectomies or decompressions
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Single blind
- Primary purpose
- Treatment
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT07408726 · Mono vs polyaxial PHS