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临床试验/NCT06024785
NCT06024785招募中不适用

Comparison of Ligamentous Fixation Technique (Vertebropexy) Versus Conventional Decompression or Fusion Surgery for Degenerative Lumbar Spinal Disease: A Randomized Controlled Trial

Balgrist University Hospital2 个研究点 分布在 1 个国家目标入组 164 人开始时间: 2025年1月16日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
164
试验地点
2
主要终点
ODI (Oswestry Disability Index)

研究概览

简要总结

To assess the need for additional fusion surgery versus the risk of a revision surgery in patients with degenerative lumbar spinal disease and to assess efficacy and risk of the ligamentous fixation technique (vertebropexy)

详细描述

The global share of people over the age of 65 years has been consistently on the rise over the past few decades, and is still projected to increase. The increasing life expectancy, overall advances in medical care and therefore, the higher average age of people seeking surgical treatment lead to increasing numbers of spine surgeries: Spinal fusion is one of the most frequently used surgical treatment modalities for spinal disorders with 7.6 million per year worldwide (EU: 700,000, USA: 450,000, CH: 9000) and provides stability by internal rigid fixation of the spine with screws, rods and bony fusion. Although producing reliable short-term results with rapid pain relief and positive effects on patient outcome, implant-related complications, painful pseudarthrosis (non-union of bone), screw loosening, and adjacent segment disease lead to one-third of patients requiring reoperation within 15 years. These complications might be evoked by altered biomechanics with redistribution of loads and subsequently increased stress at the bone-implant interface as well as long fusions leading to relevant, irreversible loss of motion. Therefore, a new treatment modality which reinforces bony spinal segments with ligaments, the so called "vertebropexy", was recently developed by Farshad et al. The goal is to achieve targeted stabilization of the spine by inserting ligamentous allografts to counteract instability, without immobilizing the segment. Furthermore, it might provide additional stabilization after decompression surgery and therefore reduce revision surgery rates due to instability in clinically relevant directions as flexion-extension or anterior shear stress. However, to become a broadly accepted surgical alternative to existing surgical techniques for degenerative lumbar spinal disease like dorsal fusion and spinal decompression surgery, the new technique must provide convincing long-term results superior to those of these established procedures which is the primary objective of this randomized controlled trial.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

盲法说明

There is no blinding.

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age ≥ 18 years
  • Single-level or two-level lumbar surgery needed
  • Indication for decompression surgery in patients with spinal canal stenosis and additional stable degenerative listhesis (without facet joint effusion ≥ 2mm)
  • Indication for fusion surgery in patients with spinal canal stenosis and additional unstable degenerative listhesis (facet joint effusion ≥ 2mm), in patients with foraminal stenosis and additional degenerative listhesis, and in patients with segment degeneration of the disc
  • Understanding in German language

排除标准

  • Indication for decompression and/or fusion surgery in patients with solely disc herniation, fractures, lytic listhesis, tumor
  • Patients undergoing revision surgery for infection
  • Patients undergoing revision surgery on the same level if bony structures have been removed (e.g. prior laminectomy or midline decompression)
  • Patients undergoing revision surgery in case of prior fusion surgery
  • Inability to understand the study for linguistic or cognitive reasons
  • Anticipated clinical follow-up of less than 6 weeks after inclusion
  • Participation in other clinical trials

研究组 & 干预措施

Indication for decompression, randomization for decompression

Active Comparator

microsurgical (i.e., the use of a microscope or magnifying glasses during decompression) lumbar laminotomy with partial removal of the medial facet joint by preserving the midline structures (supraspinous-interspinous ligament complex); approach: bilateral or ipsilateral with cross-over to the contralateral side

干预措施: Vertebropexy (Procedure)

Indication for decompression, randomization for vertebropexy

Experimental

decompression (see above) and additional stabilization of the spine with a ligament (for instance semitendinosus donor allograft), which connect the postoprior structures (Proc. Spinosus and/or Lamina) of the vertebrae . Situation-related application of laminar bands or analogous suture material (for instance FiberTape, Arthrex, Naples or Nile Band, K2M, Virginia)

干预措施: Vertebropexy (Procedure)

Indication for fusion, randomization for fusion

Active Comparator

decompression (see above) and posterolateral instrumented fusion (arthrodesis) with implantation of pedicle screws, titanium alloy rods across the level of listhesis, an intervertebral fusion device and local autograft as well as DBX (demineralized bone matrix) to improve bony fusion

干预措施: Vertebropexy (Procedure)

Indication for fusion, randomization for vertebropexy

Experimental

decompression (see above) and additional stabilization of the spine with a ligament (for instance semitendinosus donor allograft), which connect the postoprior structures (Proc. Spinosus and/or Lamina) of the vertebrae . Situation-related application of laminar bands or analogous suture material (for instance FiberTape, Arthrex, Naples or Nile Band, K2M, Virginia)

干预措施: Vertebropexy (Procedure)

结局指标

主要结局

ODI (Oswestry Disability Index)

时间窗: 2 years postoperative

To assess and compare the clinical outcome of patients with spinal canal stenosis or foraminal stenosis +/- degenerative listhesis with either vertebropexy, decompression or fusion surgery

次要结局

  • Revision surgery(2 years postoperative)
  • Duration of surgery(Perioperative)
  • Length of hospital stay(Perioperative)
  • VAS (Visual Analogue Scale)(2 years postoperative)
  • SSM satisfaction (Spinal Stenosis Measure)(2 years postoperative)
  • EQ-5D (European Quality of Life Five Dimension)(2 years postoperative)
  • Intraoperative blood loss(Perioperative)
  • SSM symptoms/function (Spinal Stenosis Measure)(2 years postoperative)
  • Use of analgesia(2 years postoperative)
  • Use of physical therapy(2 years postoperative)
  • Complications(2 years postoperative)

研究者

发起方
Balgrist University Hospital
申办方类型
Other
责任方
Sponsor

研究点 (2)

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