跳至主要内容
临床试验/DRKS00013063
DRKS00013063进行中(未招募)不适用

Prospective, Open, Non-randomized, Non-interventional Explorative, Comparative, Uncontrolled Cohort Study for Post Market Clinical Follow-Up of the BPK-S Integration UC in the Variants CoCr or Ceramic as Primary Implant - 2017-02-BPK-S Comparison

PETER BREHM GmbH0 个研究点目标入组 28 人开始时间: 2018年2月15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
28

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 Years 至 one(—)
性别
All

入选标准

  • *Congenital or acquired knee joint defects/deformation
  • *Defects or malfunction of the knee joint
  • *Arthrosis (degenerative, rheumatic)
  • *Post-traumatic arthritis
  • *Symptomatic knee instability
  • *Reconstruction of flexibility
  • *Patients with metal hypersensitivity (ceramic tibia/femur)

排除标准

  • *Illnesses which can be treated without using a knee joint implant.
  • *Acute or chronic infections near the implantation
  • *Systemic diseases and metabolic disorders
  • *Serious osteoporosis
  • *Serious damage to the bone structures that impedes stable implantation of the implant components
  • *Diseases that impair bone growth, e.g. cancer, renal dialysis, osteopenia, etc.
  • *Bone tumors in the area of the implant anchoring
  • *Obesity or overweight of the patient
  • *Overload of the knee implant to be expected
  • *Abuse of medication, drug abuse, alcoholism or mental disease
  • *Pregnancy
  • *Lack of patient cooperation
  • *Sensitivity to foreign matter in the implant materials
  • *Patients under the age of 18
  • *Patients participating in another trial

研究者

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