NL-OMON34366已完成不适用
Feasibility study to evaluate the clinical outcome of the Scorpio knee prosthesis following THE LAZIRUSH CONCEPT - Lazirush study
Stryker SA0 个研究点目标入组 50 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
- 50
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 至 99（—）
入选标准
- •A.Patients willing to sign the EC approved, study specific Informed Patient Consent Form.
- •B.Patients willing and able to comply with scheduled postoperative clinical and radiographic evaluations and rehabilitation.
- •C.Patients requiring a primary unilateral total knee replacement.
- •D.Patients with ASA Physical status 1 &2.
- •E. Patients having a partner at home for assistence.
排除标准
- •A.Patients with Rheumatoid arthritis, insulin dependent diabetes, severe osteoporosis, or an inflammatory cause for osteoarthritis.
- •B.Patients with other lower limb problems than their planned primary unilateral total knee arthroplasty.
- •C.Patients requiring revision knee surgery.
- •D.Patients with ASA physical status more than 2.
- •E.Patients requiring bilateral total knee replacement
研究者
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