跳至主要内容
临床试验/NCT04337151
NCT04337151Unknown不适用

Blood Titanium Analysis of Patients With MAGEC Spine Rods in the COVID-19 Environment

Royal National Orthopaedic Hospital NHS Trust1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2020年4月最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
100
试验地点
1
主要终点
Titanium level

研究概览

简要总结

Magnetic Expansion Control (MAGEC) growth rods are used in the surgical treatment of children with scoliosis; the primary constituent metal alloy in these is titanium.

Since June 2019, the manufacturer has released two Urgent Field Safety Notices (FSN) relating to known issues with the function of the rods that increase the risk of early failure and unplanned revisions. The UK MHRA has issued two similar Medical Device Alerts (MDA) with the most recent MDA issued on 1st April 2020, stating that (1) MAGEC rods must not be implanted in the UK until further notice and (2) all patients already implanted with this device should be followed up as soon as is possible.

At the time of writing, hospitals across the world are facing incredible challenges in dealing with the COVID-19 pandemic. Due to this, virtually all planned clinic visits for MAGEC rod patients and X-ray appointments have been postponed to help reduce the risk of the virus spreading.

Recent retrieval studies have shown that mechanical wear and corrosion of these rods is common, with a risk that the debris generated is released into surrounding tissue. This wear and corrosion is thought to be the primary cause of implant failures and the underlying implant factors leading to the issuing of FSNs and MDAs.

Whilst titanium is known to be highly biocompatible, the baseline and toxic levels of this alloy in biological fluids are poorly understood. Additionally, a better understanding of blood titanium levels in patients with MAGEC rods may enable this to become a biomarker of wear and corrosion of the rods. This may help surgeons identify earlier those patients who may develop implant related problems.

Furthermore, in the current COVID-19 environment, a blood test to measure titanium levels may be one of the most suitable ways in which to continue patient monitoring (and identify those at greatest risk of implant related issues), in the absence of regular clinic visits.

Previous work from the RNOH involved a similar study investigating patients with titanium hip implants.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Retrospective

入排标准

性别
All
接受健康志愿者

入选标准

  • Patients that have been treated with, and still have, a MAGEC rod.

排除标准

  • Patients that do not have a MAGEC rod implant.

结局指标

主要结局

Titanium level

时间窗: Within 6 months

次要结局

未报告次要终点

研究者

发起方
Royal National Orthopaedic Hospital NHS Trust
申办方类型
Other
责任方
Principal Investigator
主要研究者

Dr Harry Hothi

Implant Science Fellow

Royal National Orthopaedic Hospital NHS Trust

研究点 (1)

Loading locations...

相似试验

Blood Titanium Analysis of Patients With MAGEC Spine... | 临床试验