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.
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