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临床试验/NCT01124305
NCT01124305已完成4 期

A Prospective, Randomized Evaluation of Total Knee Arthroplasty Performed With Conventional and Customized Patient Instrumentation

Anderson Orthopaedic Research Institute1 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2010年5月1日最近更新:
适应症
干预措施

试验速览

阶段
4 期
状态
已完成
入组人数
70
试验地点
1
主要终点
Length of Surgery

研究概览

简要总结

The main purpose of this study is to determine whether the surgical time required for primary total knee arthroplasty is significantly less when performed with Customized Patient Instrumentation (CPI) than with conventional instrumentation. Each case will be recorded by video camera, in order to time the length of surgery and each surgical step. The number of surgical trays required for each case will be recorded. As an additional endpoint, the investigators will measure limb and component alignment on x-rays to determine if these two methods achieve equivalent alignment results. The thickness of bone cuts will be compared to the surgical plan and to each other.

The primary hypothesis is that the use of customized patient instrumentation will reduce the operative time required for total knee arthroplasty.

详细描述

Patient-specific instrumentation (PSI) has been developed for total knee arthroplasty (TKA) with several potential advantages over traditional instrumentation (TI). Shortened surgical time, fewer surgical instruments, and improved alignment are some of these proposed advantages. We sought to examine these assertions.

52 patients (26 per group) were enrolled in a prospective, randomized trial comparing CT-based PSI with TI. No difference was seen in average patient age (68 years) or BMI (31) between groups (p=0.84 and p=0.89), although there were more males in the PSI group (14 vs 7, p=0.002). A single surgeon and consistent staff performed the surgeries with the same knee prostheses, and all cases were videotaped to measure the length of surgery and each individual step. Any additional bone cuts, size changes, or ligament releases made to achieve correct alignment and balance were documented. The number of instrument trays opened for each case was recorded. Postoperative long alignment and lateral radiographs were taken to measure the coronal and sagittal plane component alignment and mechanical axis in each patient.

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

性别
All
接受健康志愿者
否

入选标准

  • •Patient requires unilateral primary total knee arthroplasty

排除标准

  • •Body mass index greater than 41
  • •Previous ipsilateral hip or ankle replacement
  • •Knee flexion contracture greater than 20 degrees

研究组 & 干预措施

Traditional Instrumentation

Active Comparator

Control group: Cases performed with traditional surgical instruments

干预措施: Traditional Instrumentation (Device)

Customized Patient Instrumentation

Experimental

Experimental group: Cases performed with custom instruments specifically made for each patient using pre-op CT scans.

干预措施: Customized Patient Instrumentation (Device)

结局指标

主要结局

Length of Surgery

时间窗: 1 day

Time elapsed from skin incision to wound closure (in seconds)

次要结局

  • Length of Each Surgical Step (in Seconds)(1 day)
  • Number of Instrument Trays Required(1 day)
  • Limb Alignment (Mechanical Axis)(4 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Nancy Parks

Knee Project Director

Anderson Orthopaedic Research Institute

研究点 (1)

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