跳至主要内容
临床试验/NL-OMON44724
NL-OMON44724已完成不适用

Multi-Center Evaluation of Post-Operative Recovery in ATTUNE Primary, Cemented Total Knee Arthroplasty - ATTUNE

DePuy Synthes Joint Reconstruction, Inc.0 个研究点目标入组 208 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
入组人数
208

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 至 99(—)

入选标准

  • a) Subject is male or female and between the ages of 22 and 80 years at the time of surgery, inclusive.
  • b) Subject was diagnosed with NIDJD resulting from osteoarthritis (OA) or post-traumatic arthritis.
  • c) Subject is a suitable candidate for cemented primary TKA using the devices described in this CIP with either resurfaced or non-resurfaced patellae.
  • d) Subject has given voluntary, written informed consent to participate in this clinical investigation and has authorized the transfer of his/her information to DePuy Synthes Joint Reconstruction (see Section 6.3.2).
  • e) Subject is currently not bedridden
  • f) Subject, in the opinion of the Investigator, is able to understand this clinical investigation and is willing and able to perform all study procedure and follow-up visits and co-operate with investigational procedures.
  • g) Subject is able to speak, read, and comprehend the Informed Consent Document as well as complete the PROs in the CIP in either Dutch or English translations.

排除标准

  • a) The Subject is a woman who is pregnant or lactating.
  • b) Contralateral knee has already been enrolled in this study.
  • c) Subject had a contralateral amputation.
  • d) Previous partial knee replacement (unicompartmental, bicompartamental or patellofemoral joint replacement), patellectomy, high tibial osteotomy or primary TKA in affected knee.
  • e) Subject is currently experiencing radicular pain from the spine that radiates into the limb to receive TKA.
  • f) Subject has participated in a clinical investigation with an investigational product (drug or device) in the last three months.
  • g) Subject is currently involved in any personal injury litigation, medical-legal or worker*s compensation claims.
  • h) Subject, in the opinion of the Investigator, is a drug or alcohol abuser (in the last 5 years) or has a psychological disorder that could affect their ability to complete patient reported questionnaires or be compliant with follow-up requirements.
  • i) Subject was diagnosed and is taking prescription medications to treat a muscular disorder that limits mobility due to severe stiffness and pain such as fibromyalgia or polymyalgia.
  • j) Subject has a significant neurological or musculoskeletal disorder(s) or disease that may adversely affect gait or weight bearing (e.g. muscular dystrophy, multiple sclerosis, Charcot disease).
  • k) Subject is suffering from inflammatory arthritis (e.g. rheumatoid arthritis, juvenile rheumatoid arthritis, psoriatic arthritis, systemic lupus erythematosus, etc.).
  • l) Subject has a medical condition with less than 3 years of life expectancy.

研究者

发起方
DePuy Synthes Joint Reconstruction, Inc.

相似试验

Multi-Center Evaluation of Post-Operative Recovery... | 临床试验