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临床试验/ISRCTN17022568
ISRCTN17022568已完成未知

Scorpio NRG, Triathlon Total Knee, Triathlon PKR with X3 Insert International Multicentre Outcomes Register

Stryker European Operations BV (Netherlands)0 个研究点目标入组 1,600 人开始时间: 2013年3月22日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
1,600

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

性别
All

入选标准

  • 1. Patients requiring primary Total Knee Arthroplasty (TKA), suitable for the use of the Scorpio NRG with X3 insert or Triathlon Total Knee System with X3 insert, or, patients requiring partial knee resurfacing (unicompartmental knee) suitable for the use of the Triathlon PKR (Partial Knee Resurfacing) System with X3 insert
  • 2. Patients who understand the conditions of the outcomes registry and are willing and able to comply with the standard post-operative evaluations and the prescribed rehabilitation
  • 3. Patients who signed the Informed Consent Form (approved by Ethics Committee if required) prior to surgery

排除标准

  • Does not meet inclusion criteria

研究者

发起方
Stryker European Operations BV (Netherlands)

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