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临床试验/NCT05291754
NCT05291754进行中(未招募)不适用

3D Printed PEEK Implants for Cranioplasty

Skane University Hospital2 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2021年11月26日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
40
试验地点
2
主要终点
Performed PEEK implants

研究概览

简要总结

This study is a non-randomised and single center study with patients needing an artificial skull bone eg cranioplasty. 40 patients will be implanted with in house manufactured polyether ether ketone (PEEK) implants using a fused filament fabrication 3D printer. The primary aim is to ascertain safety and feasibility of the procedure. The secondary aim is to compare complication rates with conventional methods such as autologous bone and polymethylmetacrylate (PMMA).

详细描述

Cranioplasty is the surgical repair of a congenital or cranial defects after head trauma, infection or decompressive craniectomy. Although some patients can tolerate cranial defects for varied periods of time, cranioplasty is mostly indicated due to the increased risk of additional brain trauma, local pain or impaired CSF circulation but also aesthetic and psychological issues. The gold standard for repair since many years is cranioplasty with autologous bones . However, sometimes it not feasible to use the patient's autologous bone due to infections, trauma, bone graft resorption and donor-site morbidity. To replace the autologous bone grafts several different materials have been used, or are in use, as titanium meshes, hydroxyapatite cement and plastic resins as polymethyl methacrylate (PMMA) and porous polyethylene. Some of these have gathered increased interest due to advancements in technology for manufacture of these materials, and also the possibility to create custom made implants or moulds.

The present study aims to assay safety and feasibility of in house 3D printed medical grade PEEK implants in research persons with acquired skull defects.

The implants will be manufactured after 3D rendering from CT images of the skull defects, sterilised and aseptically inserted in the defects by means of a surgical intervention.

A safety interim analysis will be performed after inclusion of 10 patients.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

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

  • Scheduled for cranioplasty
  • Informed consent

排除标准

  • No informed consent
  • Implant size greater than 12x12 cm

结局指标

主要结局

Performed PEEK implants

时间窗: At end of surgical procedure, up to 2 months after inclusion

Percentage of performed PEEK implants out of included patients.

Safety of PEEK implants

时间窗: 1 year

Survival percentage of PEEK implants. Will be compared to historical PMMA and autologous bone implants.

次要结局

  • Exposure time of PEEK implants compared to PMMA implants.(During surgical procedure, up to 2 months after inclusion.)
  • Complications of PEEK implants(12 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Peter Siesjö

Professor

Skane University Hospital

研究点 (2)

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