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临床试验/NCT03511144
NCT03511144撤回不适用

A Prospective Randomised Double Blind Single Centre Study Comparing Measured Resection and Ligament Balancing Implantation Techniques Using the Unity Knee™ Total Knee System

Corin0 个研究点开始时间: 2018年7月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
撤回
发起方
Corin
主要终点
Posterior condylar offset (PCO)

研究概览

简要总结

A comparison of two Unity Knee™ tissue-balancing techniques by analysing the results from X-rays and patient questionnaires.

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
Double (Participant, Outcomes Assessor)

入排标准

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

入选标准

  • Subjects suitable for the Unity Knee™ Total Knee System according to the product "Instructions for use"
  • Over 18 years old
  • Male and female subjects who are skeletally mature
  • Subjects who have a smartphone (iOS or Android) with internet connection via mobile Internet data or Wi-Fi connection
  • Subjects able to understand what is expected of them and be able to comply with the study protocol requirements

排除标准

  • Any subject listed for a revision total knee replacement or conversion of a unicondylar replacement to a total knee replacement on the operative knee
  • Any subject with fixed flexion contracture greater than 20 degrees
  • Any subject with varus/valgus deformity greater than 15 degrees
  • Any subject with confirmed osteoarthritis or other pathologies affecting the contralateral knee that is anticipated to require surgery within 12 months
  • Any subjects with contralateral knee replacement that is anticipated to require revision surgery within 12 months
  • Any subject whose prospects for a recovery to independent mobility would be compromised by known co-existent, medical problems
  • Any subject with a known sensitivity to device material
  • Any subject who is pregnant
  • Any subject currently a prisoner
  • Any subject known to be a drug or alcohol abuser, or have a psychological disorder that could affect follow-up care or treatment outcomes
  • Any subject currently involved in any personal injury litigation, medical-legal or worker's compensations claims
  • Any subject unable to read and understand English

研究组 & 干预措施

Measured resection

Active Comparator

Total knee replacement using the Unity Knee™ implanted with the measured resection surgical technique

干预措施: Unity Knee™ TKR using measured resection (Device)

Ligament balancing

Active Comparator

Total knee replacement using the Unity Knee™ implanted with the ligament balancing surgical technique

干预措施: Unity Knee™ TKR using ligament balancing (Device)

结局指标

主要结局

Posterior condylar offset (PCO)

时间窗: 6 weeks post-op

Any difference in PCO from preoperative to 6 weeks post-surgery

次要结局

  • Oxford Knee Score (OKS)(Up to 24 months post-op)
  • Joint line in extension(6 weeks post-op)
  • Joint line in flexion(6 weeks post-op)
  • Femoral flexion angle(6 weeks post-op)
  • Distal femoral component angle(6 weeks post-op)
  • Tibial component angle(6 weeks post-op)
  • Tibial slope(6 weeks post-op)
  • Hip-knee-ankle (HKA) angle(6 weeks post-op)
  • Knee injury and Osteoarthritis Score - Physical Function Shortform (KOOS-PS)(Up to 24 months post-op)
  • Hospital Anxiety and Depression Scale (HADS)(Up to 6 months post-op)
  • EuroQoL 5-dimension health state (EQ-5D 5-level)(Up to 6 months post-op)

研究者

发起方
Corin
申办方类型
Industry
责任方
Sponsor

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