ISRCTN51839535已完成未知
Feasibility study to evaluate the clinical outcome of the Scorpio knee prosthesis following the Lazirush concept
Stryker SA (Switzerland)0 个研究点目标入组 50 人开始时间: 2013年8月6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
- 50
研究概览
简要总结
2018 results in: https://www.ncbi.nlm.nih.gov/pubmed/30027483 [added 17/01/2019]
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- All
入选标准
- •1. Patients willing to sign the informed patient consent form.
- •2. Patients willing and able to comply with scheduled postoperative clinical and radiographic evaluations and rehabilitation.
- •3. Patients requiring a primary unilateral total knee replacement.
- •4. Patients with American Society of Anesthesiologists (ASA) Physical status 1 & 2.
- •5. Patients having a partner at home for assistance.
排除标准
- •1. Patients with Rheumatoid arthritis, insulin-dependent diabetes, severe osteoporosis, or an inflammatory cause for osteoarthritis.
- •2. Patients with other lower limb problems than their planned primary unilateral total knee arthroplasty.
- •3. Patients requiring revision knee surgery.
- •4. Patients with ASA physical status more than 2.
- •5. Patients requiring bilateral total knee replacement.
研究者
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