跳至主要内容
临床试验/NL-OMON40356
NL-OMON40356已完成不适用

Persona Outcomes Led Assessment Research in Total Knee Arthroplasty - POLAR

Zimmer GmbH0 个研究点目标入组 50 人开始时间: 待定最近更新:
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

发起方
Zimmer GmbH

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