NL-OMON40356已完成不适用
Persona Outcomes Led Assessment Research in Total Knee Arthroplasty - POLAR
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- Zimmer GmbH
- 入组人数
- 50
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 至 99(—)
入选标准
- •1. Patient is 18 to 75 years of age, inclusive
- •2. Patient qualifies for a 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:
- •a. Rheumatoid arthritis, osteoarthritis, traumatic arthritis, polyarthritis
- •b. Collagen disorders and/or avascular necrosis of the femoral condyle
- •c. Post-traumatic loss of joint configuration, particularly when there is patellofemoral
- •erosion, dysfunction or prior patellectomy
- •d. Moderate valgus, varus, or flexion deformities
- •e. The salvage of previously failed surgical attempts that did not include
- •partial or total knee arthroplasty of the ipsilateral knee
- •3. Patient is willing and able to provide written Informed Consent by signing and dating
- •the EC approved Informed Consent form
- •4. Patient is willing and able to complete scheduled study procedures and follow-up
- •evaluations
- •5. Independent of study participation, patient is a candidate for commercially available
- •Zimmer Persona knee implants implanted in accordance with product labeling
排除标准
- •1. Patient is currently participating in any other surgical intervention studies or pain
- •management studies
- •2. Previous history of infection in the affected joint and/or other local/systemic infection
- •that may affect the prosthetic joint
- •3. Insufficient bone stock on femoral or tibial surfaces
- •4. Skeletal immaturity
- •5. Neuropathic arthropathy
- •6. Osteoporosis or any loss of musculature or neuromuscular disease that compromises
- •the affected limb
- •7. Stable, painless arthrodesis in a satisfactory functional position
- •8. Severe instability secondary to the absence of collateral ligament integrity
- •9. Rheumatoid arthritis accompanied by an ulcer of the skin or a history of recurrent
- •breakdown of the skin
- •10. Patient has a known or suspected sensitivity or allergy to one or more of the implant
- •11. Patient is pregnant or considered a member of a protected population (e.g., prisoner,
- •mentally incompetent, etc.)
- •12. Patient has previously received partial or total knee arthroplasty for the ipsilateral
研究者
相似试验
尚未招募
不适用
Study On Quality Outcomes In Burn PatientsCTRI/2018/01/011564Department of Hospital Administration
已完成
不适用
An audit of assessment and treatment adequacy of pain in cancer patients in casualty at Tata Memorial HospitalCTRI/2011/08/001979Department of Anaesthesiology Critical care Pain100
尚未招募
Unknown
Development and validation of outcome measure to assess the physical activity preparedness in patients with one sided body weakness or paralysis.CTRI/2024/04/066316Department of Physiotherapy
尚未招募
2 期
Efficacy of Homoeopathy in Management of Adjustment Disorder with help of Synthesis Repertory.CTRI/2023/04/051264Parul University
尚未招募
Unknown
Factors affecting the involvement of working parents in learning activities of children.CTRI/2023/06/054268Ms Dilshad Abbas Ali
