跳至主要内容
临床试验/NCT03905174
NCT03905174招募中不适用

A Randomised, Single Blind Study Assessing Radiological Outcomes for Massive Segmental Femoral Replacements Using Either Porous Collar or Porous Collar With HA or Porous Collar With HA and Autologous Stem Cells

Iva Hauptmannova2 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2018年9月20日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
30
试验地点
2
主要终点
Radiological outcomes (X-ray, CT)

研究概览

简要总结

The study will review the use of massive segmental replacements in the femur, which have a porous collar with and without HA, and autologous stem cell augment. This is a randomised controlled trial.

详细描述

The current surgical treatment of bone cancer patients and revision limb salvage requires usage of massive endoprosthetic bone implants. The incidence of aseptic loosening is a major cause of prosthesis failure in these patients, exploring ways to reduce such failures would allow extending longevity of massive implants in a relatively young population.

Current published literature stipulates that osteointegration could improve longevity of massive implants. Evidence suggests that usage of osteointegrated hydroxyapatite (HA) coated collar would reduce the incidence of aseptic loosening around the cemented intramedullary stem in distal femoral bone prosthesis

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Single (Outcomes Assessor)

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

  • Bone cancer patients requiring primary or revision femoral segmental replacements and non-cancer patients requiring revision femoral segment replacement for aseptic loosening
  • Male or female, aged 18 years or above
  • Able to provide consent

排除标准

  • unable/unwilling to consent
  • revisions surgery due to infection
  • bone cancer patients excluded from stem cell arm
  • bone cancer patients with pathological fractures

结局指标

主要结局

Radiological outcomes (X-ray, CT)

时间窗: at 2 years (+/- 2 weeks)

radiological outcomes to determine integration of implant into bone - bone growth

次要结局

  • Visual Analogue Score (VAS) pain score(up to 2 years (+/- 2 weeks))

研究者

发起方
Iva Hauptmannova
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Iva Hauptmannova

Head of Research & Innovation

Royal National Orthopaedic Hospital NHS Trust

研究点 (2)

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