DRKS00017483已完成不适用
A prospective PMCF multicentre study analysing performance and safety outcome of the Affinis Glenoid vitamys uncemented in total shoulder arthroplasty
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 75
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 Years 至 one（—）
- 性别
- All
入选标准
- •Informed consent form (signed by participant and investigator)
- •- Primary implantation
- •- Primary osteoarthritis, secondary osteoarthritis, fracture sequelae, avascular
- •necrosis of the humeral head
- •- Age at inclusion >18 years
- •- Intact rotator cuff
- •- Preoperative Constant Score >20 points
- •- Glenoid <15° retroversion and <70% humeral head subluxation
排除标准
- •-Missing consent
- •- Rheumatoid arthritis
- •- Known or suspected non-compliance (e.g. drug or alcohol abuse)
- •- Revision surgery
- •- Presence of sepsis or malignant tumours
- •- Chemotherapy treatment within 6 months before surgery
- •- >5mg/day of corticosteroids, excluding inhalers, within 3 months before surgery
- •- Women who are pregnant or breast feeding
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