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临床试验/NCT03893110
NCT03893110撤回不适用

Carbon PEEK Versus Titanium Pedicle Screws in the Treatment of Spinal Tumors - A Randomized Controlled Trial

Balgrist University Hospital2 个研究点 分布在 1 个国家开始时间: 2018年6月27日最近更新:
适应症

试验速览

阶段
不适用
状态
撤回
发起方
试验地点
2
主要终点
radiation dose

研究概览

简要总结

Radiation therapy is a cornerstone in the treatment of spinal neoplasms as radical resections are often limited anatomically. Frequently, a surgical stabilization with implants is required. However, metallic implants not only make the CT-based planning of a subsequent radiation therapy more difficult, but might also have an uncontrolled dose modulating effect in adjuvant radiotherapy. At the spine, radiation is limited by the effective dose posed to the relatively radiosensitive spinal cord. While metallic implants might result in an inhomogeneous and uncontrollable dose distribution due to the interface effect, the use of new radiolucent implants consisting of carbon/polyether ether ketone (PEEK) might allow a more homogeneous and predictable dose distribution. This study aims to evaluate the potential benefits of the use of carbon/PEEK pedicle screws during adjuvant radiation therapy and follow-up imaging of spinal tumors.

60 patients will randomized 1:1 into either treatment arm (Pedicle System Carbon/PEEK vs. Pedicle System Titanium). The feasibility of planning the radiation therapy will be evaluated. The postoperatively administered total radiation dose is documented. The radiological visualization of the area of interest will be evaluated The surgical outcome is evaluated by fusion rate, implant integrity and anchorage. Patients will be followed up for 12 months according to local standards.

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
Single (Participant)

入排标准

年龄范围
18 Years 至 99 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients 18 to 99 years of Age
  • Primary and secondary spinal tumors of the thoracolumbar spine requiring posterior instrumentation and radiation therapy

排除标准

  • Need of cement augmentation or anterior cage support (corpectomy)
  • Patients with contraindication against surgical resection
  • Patients with incomplete medical records or insufficient imaging

结局指标

主要结局

radiation dose

时间窗: within 6 weeks of radiation therapy

The total radiation dose administered is measured in Gray

feasibility of planning the radiation therapy

时间窗: before radiation therapy

evaluated by a subjective score (0-10) stated by an independent radiooncologist using a visual analogue scale from 0 to 10

次要结局

  • radiological visualization of the area of interest(during radiation therapy)
  • time to recurrence(up to 1 year)

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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