跳至主要内容
临床试验/NL-OMON36696
NL-OMON36696已完成不适用

A Comparison of Signature Guides and Conventional Techniques with the Vanguard Knee System - Vanguard signature

Biomet Nederland BV0 个研究点目标入组 44 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
44

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 至 99(—)

入选标准

  • 1. Painful and disabled knee joint resulting from Osteoarthritis, Rheumatoid Arthritis or Traumatic Arthritis where one or more compartments are involved
  • 2. Correction of varus, valgus or post traumatic deformity
  • 3. Need to obtain pain relief and improve function
  • 4. Ability and willingness to follow instructions, including control of weight and activity level, and to return for follow-up evaluations
  • 5. Good nutritional state of the patient
  • 6. Full skeletal maturity of the patient
  • 7. Patients are at least 18 years of age
  • 8. Patients of either sex
  • 9. Consent form read, understood, and signed by patient.
  • 10. Able to obtain MRI

排除标准

  • 1. Absolute contraindications include: infection, sepsis, osteomyelitis and a previous joint replacement.

研究者

发起方
Biomet Nederland BV

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