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临床试验/NCT03676179
NCT03676179已完成不适用

The Comparison of Anterior Knee Pain in Patella With or Without Denervation in Medial Unicompartmental Knee Arthroplasty

Ramathibodi Hospital1 个研究点 分布在 1 个国家目标入组 66 人开始时间: 2018年3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
已完成
入组人数
66
试验地点
1
主要终点
Kujala score

研究概览

简要总结

the present study will conduct to assess anterior knee pain and complications after medial UKA with or without patella denervation in medial compartment arthritis and severe lateral facet patellofemoral arthritis patients.

详细描述

In this prospective cohort study, the investigators will conduct to compare the clinical result of 70 patients of unicompartment knee arthroplasty with and without patella denervation between April, 2018 and April, 2019 for the patients with osteoarthritis.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Investigator, Outcomes Assessor)

盲法说明

unicompartment knee arthroplasty without patella denervation

入排标准

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

入选标准

  • Patients who diagnose with medial osteoarthritis (OA) of the knee with an Alhback score of 2, 3 and 4 (Ahlback 1968) and with any Kujala score for pre-operative anterior knee pain.
  • Older than 40 years of age.
  • pain on the medial joint line.
  • primary medial compartment osteoarthritis with a well preserved lateral compartment with competent cruciate ligaments with correctable intraarticular varus deformity.
  • ROM flexion up to 110° under anesthesia.

排除标准

  • Patients with fixed varus deformity > 15°
  • Inflammatory arthritis
  • Previous high tibial osteotomy or ACL reconstruction

研究组 & 干预措施

unicompartment knee arthroplasty and patella denervation

Active Comparator

UKA and patella denervation

干预措施: patella denervation (Procedure)

unicompartment knee arthroplasty and patella non-denervation

Experimental

UKA and patella non-denervation

干预措施: patella non-denervation (Procedure)

结局指标

主要结局

Kujala score

时间窗: 6 months

Kujala score including 13 parameters with the score of 0-100, the higher the score the better the function.

次要结局

  • complication(6 months)

研究者

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

Jatupon Kongtharvonskul

principle investigator

Ramathibodi Hospital

研究点 (1)

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