跳至主要内容
临床试验/NCT06019832
NCT06019832进行中(未招募)不适用

Analysis of Varus Collapse in Obese Patients With Stem and Non-Stem Tibial Components Following Primary Total Knee Arthroplasty

Jacob M. Elkins1 个研究点 分布在 1 个国家目标入组 54 人开始时间: 2023年8月14日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
54
试验地点
1
主要终点
Varus Collapse

研究概览

简要总结

The purpose of this study is to compare rates of varus collapse, aseptic loosening, and implant failure in female obese patients undergoing total knee arthroplasty (TKA) and will review the degree of influence of stemmed tibial components versus non-stemmed tibial components on varus collapse and aseptic loosening, a consequence of implant micromotion.

详细描述

The purpose of this study is to identify varus collapse, aseptic loosening, and implant failure in female obese patients undergoing total knee arthroplasty (TKA). In addition, this study will review the degree of influence of stemmed tibial components versus non-stemmed tibial components on varus collapse and aseptic loosening, a consequence of implant micromotion.

Female patients age 40 and older with BMI of 35 kg/m2 and above will be randomized into two groups: the non-stem tibial component (control group) and the stem tibial component (treatment group). Previous studies done in the past in normal weight patients showed that there is little or no advantage in using the stem tibial implants over the non-stem ones. Theoretically, biomechanical studies have suggested that there may be improved fixation and load distribution with the use of stem tibial implants. Thus, it is necessary to see if there is any difference between both implant options among female patients who have the highest incidence of varus collapse. In terms of design, the stem tibial implants are slightly longer than the non-stem ones. They are designed to extends deeper into the tibia to enhance fixation and improve load distribution. The use of either stem tibial implants is usually based on patients' characteristics and surgeons' preference.

Following informed consent, standard perioperative patient-reported metrics will be collected (Knee Injury and Osteoarthritis Outcome Score for Joint Replacement [KOOS-JR], American Knee Society score, and Patient-Reported Outcome Measurement Information System 10 [PROMIS-10]) before surgery and after surgery (2-3 weeks, 8-10 weeks, 1 year, 3 years, and 5 years). After surgery, study participants will receive routine surgical care which includes two knee radiographs at 8-10 weeks and one year. In addition to this, the study participants will be evaluated at 3 years, and 5 years postoperative periods where they will complete routine PROMs as listed above and have knee radiographs during each visit.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
40 Years 至 99 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Female adult patients with severe osteoarthritis scheduled to have primary total knee arthroplasty
  • Age 40 or older
  • 35 kg/m2 and above
  • Only patients from the PI's clinic will be included.
  • Women who are still menstruating and are currently on contraceptives and women who are in menopause.

排除标准

  • Patients who have some active local or widespread infection (including secondary or inflammatory osteoarthritis)
  • medical conditions that put them at risk of complications or death during and after the study would not be eligible for surgery
  • Patients with previous knee surgery on arthroplasty site will be excluded
  • Pregnant patients and women who are capable of getting pregnant

研究组 & 干预措施

Group A: Stemmed Tibial Implant

Active Comparator

This study group will receive a stemmed tibial implant as part of their TKA.

干预措施: Stemmed Tibial Implant (Device)

Group B: Non-Stemmed Tibial implant

Active Comparator

This study group will receive a non-stemmed tibial implant as part of their TKA.

干预措施: Total Knee Arthroplasty (TKA) (Procedure)

Group B: Non-Stemmed Tibial implant

Active Comparator

This study group will receive a non-stemmed tibial implant as part of their TKA.

干预措施: Non-stemmed tibial implant (Device)

Group A: Stemmed Tibial Implant

Active Comparator

This study group will receive a stemmed tibial implant as part of their TKA.

干预措施: Total Knee Arthroplasty (TKA) (Procedure)

结局指标

主要结局

Varus Collapse

时间窗: up to 5 years post surgery

The investigators will track rate of varus collapse.

Aseptic loosening

时间窗: up to 5 years post surgery

The investigators will track rates of aseptic loosening.

次要结局

未报告次要终点

研究者

发起方
Jacob M. Elkins
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Jacob M. Elkins

Assistant Professor

University of Iowa

研究点 (1)

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