Zimmer Biomet Shoulder Arthroplasty Long-term Post Market Clinical Follow-up Study
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 584
- 试验地点
- 34
- 主要终点
- Frequency and Incidence of Adverse Events (Safety)
研究概览
简要总结
The objectives of this study are to confirm the safety, performance, and clinical benefits of Zimmer Biomet Shoulder Arthroplasty Systems and its instrumentation in primary or revision shoulder arthroplasty. These objectives will be assessed using standard scoring systems, radiographic evidence, and adverse event records. Safety of the system will be assessed by monitoring the frequency an incidence of adverse events.
详细描述
The primary endpoint is defined as survival of the implant at 10 years, which is based on removal or intended removal of at least 1-study implant component and will be determined by using the Kaplan Meier method. The safety of the system will be assessed by monitoring the frequency and incidence of adverse events. Separate analysis will be done for each arm of the study.
The secondary endpoint is represented by the performance and clinical benefits of Zimmer Biomet Shoulder Arthroplasty Systems and its instrumentation after 2 years, which will be assessed by the American Shoulder and Elbow Surgeons (ASES) shoulder score. The secondary endpoint evaluation will also assess the overall pain, functional performance, quality of life and radiographic parameters of all enrolled study subjects.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 20 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patient must be 20 years of age or older.
- •Patient must be anatomically and structurally suited to receive shoulder arthroplasty implants.
- •Patient is a candidate for shoulder arthroplasty due to one or more of the following:
- •Non-inflammatory degenerative joint disease including osteoarthritis and avascular necrosis.
- •Rheumatoid arthritis.
- •Correction of functional deformity.
- •Fractures of the proximal humerus, where other methods of treatment are deemed inadequate.
- •Difficult clinical management problems, where other methods of treatment may not be suitable or may be inadequate.
- •Patient must be able and willing to complete the protocol required follow-up.
- •Patient must be able and willing to sign the IRB/EC approved informed consent.
- •Patient has grossly deficient rotator, (for reverse application)
- •With severe arthropathy and/or
- •Previously failed shoulder joint replacement
- •Patient must have functional deltoid muscle (for reverse application)
排除标准
- •Patient is unwilling or unable to give consent or to comply with the follow-up program.
- •Patient has any condition which would in the judgement of the Investigator, place the patient at undue risk or interfere with the study.
- •Patient is known to be pregnant or breastfeeding.
- •Patient is a vulnerable subject (prisoner, mentally incompetent or unable to understand what participation to the study entails, a known alcohol or drug abuser, and/or anticipated to be non-compliant).
- •Patient is uncooperative or patient with neurologic disorders who is incapable or unwilling to follow directions.
- •Patient has any sign of infection affecting the shoulder joint or in its proximity which may spread to the implant site.
- •Patient has rapid joint destruction, marked bone loss, or bone resorption apparent on roentgenogram.
- •Patient has any neuromuscular disease compromising the affected limb that would render the procedure unjustifiable.
- •Patient presents with osteoporosis, which in the opinion of the Investigator, may limit the subject's ability to support total shoulder arthroplasty using the study device.
- •Patient has osteomalacia.
- •Patient has a metabolic disorder that may impair bone formation.
- •Patient has deficient rotator cuff.
- •Patient presents with significant injury to the upper brachial plexus.
- •Patient has paralysis of the axillary nerve.
- •Patient has non-functional deltoid or external rotator muscles.
研究组 & 干预措施
Zimmer Biomet Total Shoulder Arthroplasty System
Patients who are having primary or revision total shoulder arthroplasty who will receive a Zimmer Biomet Total Shoulder Arthroplasty System.
干预措施: Alliance Glenoid (Device)
Zimmer Biomet Total Shoulder Arthroplasty System
Patients who are having primary or revision total shoulder arthroplasty who will receive a Zimmer Biomet Total Shoulder Arthroplasty System.
干预措施: Identity Stem (Device)
结局指标
主要结局
Frequency and Incidence of Adverse Events (Safety)
时间窗: 10 years
Monitoring the frequency and incidence of adverse events, serious adverse events, adverse device effects, serious adverse device effects, and unanticipated serious adverse device effects as well as device deficiencies.
Implant Survivorship at 10 years follow-up (Kaplan Meier)
时间窗: 10 years
Based on removal or intended removal of the device and determined using the Kaplan-Meier method.
次要结局
- Clinical efficacy of the device is assessed using the American Shoulder and Elbow Surgeons (ASES) Shoulder Score at 2 years follow-up(2 years)
- Radiographic Performance [Radiolucency] at 2 years follow-up(2 years)
- Radiographic Performance [Heterotopic Ossification] at 2 years follow-up(2 years)
- Radiographic Performance [Osteolysis] at 2 years follow-up(2 years)
- Radiographic Performance [Glenoid Component Migration] at 2 years follow-up(2 year)
- Euroqol Patient Quality of life measured at 2 years follow-up (EQ-5D-5L)(2 years)
- Radiographic Performance [Humeral Component Subsidence] at 2 years follow-up(2 year)