ACTRN12609000795291撤回不适用
A prospective, multicentre, cohort study evaluating patient benefit after primary total shoulder arthroplasty with the modular PROMOS shoulder system.
Smith&Nephew Surgical Pty Ltd0 个研究点目标入组 240 人开始时间: 2009年9月15日最近更新:
试验速览
- 阶段
- 不适用
- 状态
- 撤回
- 发起方
- 入组人数
- 240
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Non-randomised trial
- 主要目的
- Treatment
入排标准
- 年龄范围
- 18 Years 至 o limit（—）
- 性别
- All
入选标准
- •1. Primary or secondary omarthrosis as an indication for primary total shoulder arthroplasty
- •2. Massive rotator cuff rupture
排除标准
- •Patients with the following critieria will be not eligible to participate in the study.
- •1. Previous ipsilateral shoulder arthroplasty
- •2. Late stage rotator cuff disease (Only for PROMOS standard prosthesis)
- •3. Acute shoulder trauma
- •4. General medical contraindication to surgery
- •5. Legal incompetence
- •6. Tumour / malignoma
- •7. Recent history of substance abuse
- •8. Any disease process that would preclude accurate evaluation (e.g.
- •neuromuscular, psychiatric or metabolic disorder)
- •9 Known hypersensitivity to the materials used
- •10. Bacterial infection at the time point of operation
研究者
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