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临床试验/NCT04321356
NCT04321356已完成不适用

Analysis of Competitive PCR and PS Total Knee Arthroplasty

The University of Tennessee, Knoxville2 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2020年2月24日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
100
试验地点
2
主要终点
Medial AP Translations, in mm, During Deep Knee Bend (DKB) Activity

研究概览

简要总结

The purpose of the study is to acquire kinematic in vivo fluoroscopy data from subjects who were implanted with Stryker Posterior Cruciate Retaining (PCR) , Stryker Posterior Stabilized (PS), Zimmer PCR, and Zimmer PS Total Knee Arthroplasty (TKAs). Our lab has previously collected data for the Smith & Nephew PCR, bi-cruciate retaining (BCR), and bi-cruciate stabilized (BCS) TKA.

详细描述

The objective for this study is to analyze the in vivo kinematics for subjects implanted with either a Stryker PCR, Stryker PS, Zimmer PCR, and Zimmer PS TKA and to compare those patterns to subjects having a normal knee from our previous study and to those patterns from subjects having a Smith & Nephew PCR, BCR, and BCS TKA.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

年龄范围
18 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Subjects will have one of the following implant types: 1) Stryker Triathlon PCR TKA (28 subjects), 2) Stryker Triathlon PS TKA (28 subjects), 3) Zimmer Persona PCR TKA (28 subjects) and 4) Zimmer Persona PS TKA (28 subjects).
  • Patients must be at least three months post-operative.
  • Participants must not experience any pain or other post-operative complications.
  • Participants must have a stable TKA and be capable of performing a deep knee bend activity.
  • Participants must weigh less than 300 lbs., not underweight (BMI < 18.5) or too obese (BMI>35).
  • Must be in the age range of 18 years to 85 years (both inclusive).
  • Participants must be able to perform the required activities without concern.
  • Subjects must be willing to sign the Informed Consent (IC) form to participate in the study.
  • Patients who do not have previous surgery on the implanted knee that might restrict their movement.

排除标准

  • Pregnant, potentially pregnant, lactating females or of childbearing age. To satisfy radiation protocol, each female subject will be asked if she is pregnant, or possibly could be pregnant. A pregnant person will not be allowed to participate in the study. (All potential female study patients will be asked if they are premenopausal or if they have undergone a hysterectomy. If the possibility of pregnancy exists, a pregnancy kit will be given to the patient at the informed consent meeting, just prior to the fluoro. Results of the test will be recorded in a test log. Any female patient showing a positive test will be excluded from testing.)
  • Subjects without the required type of knee implant.
  • Cannot have pain in other parts of the body that would prohibit the subject from performing the activities).
  • Cannot have ligamentous pain and/or laxity.
  • Unwilling to sign IC/HIPAA form(s).
  • Does not speak English.
  • Patients who have enrolled in a fluoroscopic kinematic study within the past year.
  • Patients currently involved in any personal injury litigation, medical/legal or worker's compensation claims.
  • Patients with known drug or alcohol abuse histories or psychological disorders that could affect ability to complete all aspects of the study.
  • Patients with neurological or musculoskeletal disorders that might adversely affect weight-bearing motion ability.

结局指标

主要结局

Medial AP Translations, in mm, During Deep Knee Bend (DKB) Activity

时间窗: 3 months post-operative

Anterior Posterior (AP) translations, in mm, of medial femoral condyle during deep knee bend activity. Positive values indicate anterior motion of the medial femoral condyle, and negative values indicate posterior motion of the medial femoral condyle.

Lateral AP Translations, in mm, During Deep Knee Bend (DKB) Activity

时间窗: 3 months post-operative

Anterior Posterior (AP) translations, in mm, of lateral femoral condyle during deep knee bend activity. Positive values indicate anterior motion of the lateral femoral condyle, and negative values indicate posterior motion of the lateral femoral condyle.

Maximum Flexion, in Degrees, During Deep Knee Bend Activity

时间窗: 3 months post-operative

Maximum weight-bearing flexion, in degrees, during deep knee bend activity

Axial Rotation, in Degrees, During Deep Knee Bend Activity

时间窗: 3 months post-operative

Axial rotation (AR), in degrees, during deep knee bend activity. Positive values indicate external femorotibial axial rotation, and negative values indicate internal femorotibial axial rotation.

次要结局

未报告次要终点

研究者

发起方
The University of Tennessee, Knoxville
申办方类型
Other
责任方
Principal Investigator
主要研究者

Richard Komistek

Principal Investigator

The University of Tennessee, Knoxville

研究点 (2)

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