Persona Outcomes Led Assessment Research in Total Knee Arthroplasty
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 299
- 试验地点
- 7
- 主要终点
- Knee Society Scores
研究概览
简要总结
The primary objective of this study is to obtain implant survivorship and clinical outcomes data for commercially available Persona fixed bearing knee implants used in total knee arthroplasty. The assessment will include implant survivorship and clinical performance measured by pain and function, quality of life data, radiographic parameters and survivorship.
详细描述
The study design is a prospective, multicenter, study of the commercially available Persona fixed bearing knee implants. The study will require each site to obtain Institutional Review Board (IRB) approval prior to study enrollment. All potential study subjects will be required to participate in the Informed Consent Process.
All study subjects will undergo preoperative clinical evaluations prior to their total knee arthroplasty. The post-operative clinical and radiographic evaluations will be conducted at 6 weeks, 6 months, 1 year, 2, 3, 4, and 5 years.
All info specified in the Brief Summary will be captured via the Knee Society Score, EQ-5D, Forgotten Joint Score, KSS Patient Expectations, Physical Exam, and Physician's Assessment of Radiographic Outcomes form.
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
- 18 Years 至 75 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patient 18-75 years of age, inclusive;
- •Patient qualifies for primary total knee arthroplasty based on physical exam and medical history, including diagnosis of severe knee pain and disability due to at least one of the following:
- •rheumatoid arthritis, osteoarthritis, traumatic arthritis, polyarthritis;
- •collagen disorders and/or avascular necrosis of the femoral condyle;
- •post-traumatic loss of joint configuration, particularly when there is patellofemoral erosion, dysfunction or prior patellectomy;
- •moderate valgus, varus, or flexion deformities;
- •the salvage of previously failed surgical attempts that did not include partial or total knee arthroplasty of the ipsilateral knee;
- •Patient has participated in a study-related Informed Consent process;
- •Patient is willing and able to complete scheduled study procedures and follow-up evaluations;
- •Independent of study participation, patient is a candidate for commercially available Persona fixed bearing knee components implanted in accordance with product labeling.
排除标准
- •Patient is currently participating in any other surgical intervention studies or pain management studies;
- •Previous history of infection in the affected joint and/or other local/systemic infection that may affect the prosthetic joint;
- •Insufficient bone stock on femoral or tibial surfaces;
- •Skeletal immaturity;
- •Neuropathic arthropathy;
- •Osteoporosis or any loss of musculature or neuromuscular disease that compromises the affected limb;
- •Stable, painless arthrodesis in a satisfactory functional position;
- •Severe instability secondary to the absence of collateral ligament integrity;
- •Rheumatoid arthritis accompanied by an ulcer of the skin or a history of recurrent breakdown of the skin;
- •Patient has a known or suspected sensitivity or allergy to one or more of the implant materials;
- •Patient is pregnant or considered a member of a protected population (e.g., prisoner, mentally incompetent, etc.);
- •Patient has previously received partial or total knee arthroplasty for the ipsilateral knee.
结局指标
主要结局
Knee Society Scores
时间窗: 5 years post op
This form includes alignment, instability, joint range of motion, and symptoms. The overall range of scores available is -8 to 106. A higher score indicates good alignment, range of motion, and minimal symptoms of pain. A lower score indicates poor knee alignment, potential issues in range of motion, and the likely experience of symptoms of pain.
次要结局
- Forgotten Joint Score (FJS)(5 years post-op)
- EQ-5D(5 years post op)