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临床试验/NL-OMON47889
NL-OMON47889
已完成
不适用

Knee joint (in)stability in patients with knee osteoarthritis* - Stability in Osteoarthritis (STOA)

Vrije Universiteit Medisch Centrum0 个研究点目标入组 80 人待定

概览

阶段
不适用
干预措施
未指定
疾病 / 适应症
未指定
发起方
Vrije Universiteit Medisch Centrum
入组人数
80
状态
已完成
最后更新
2年前

概览

简要总结

暂无简介。

注册库
who.int
开始日期
待定
结束日期
待定
最后更新
2年前
研究类型
Observational non invasive

研究者

入排标准

入选标准

  • In order to be eligible to participate the study, a knee osteoarthitis (KOA) subject must meet all of the following criteria:
  • \- Unilateral or bilateral diagnosis of the KOA according to the American college of Rheumatology (ACR) criteria. ACR criteria are age over 50 years, morning stiffness less than 30 minutes, crepitus on active motion, bony tenderness or absence of palpable warmth of synovium.
  • \- Able to walk for 5 minutes without stopping.
  • \- A maximal score of 7 on the numeric scale (NRS) for pain intensity during the past two weeks.
  • \- Body mass index (BMI) between 20 and 35 kg/m2\.;The KOA subjects will be assigned to the KOA\-I group (group with unstable knees) based on the following criterion:
  • \- Have had the perception of an episode of buckling, shifting or giving way of the knee in the past 4 weeks based on questionnaire (KOS\-ADLS).;The KOA subject will be assigned to the KOA\-S group (group with stable knees) based on the following criterion:
  • \- Have had no perception of an episode of buckling, shifting or giving way of the knee in the past 3 months on questionnaire (KOS\-ADLS).;Healthy controls will be age matched, gender matched and BMI matched with the total KOA group (i.e. similar mean ± standard deviation as total KOA group, except for gender which will be about the same ratio as the total KOA group (\+\- 3%)).

排除标准

  • Potential KOA subject meeting any of the following criteria will be excluded from participation in the study:
  • \- Diagnosed with hip osteoarthritis, rheumatoid arthritis or any other form of inflammatory arthritis (i.e., septic arthritis, crystal arthropathy)
  • \- Has a lower extremity joint replacement.
  • \- Has had a knee related injury last year.
  • \- Not signed an informed consent.;A potential control subject meeting any of the following criteria will be excluded from participation in the study:
  • \- Diagnosed with a musculoskeletal disease.
  • \- Has a lower extremity joint replacement.
  • \- Has had a knee related injury last five years.
  • \- Has knee\-related problems.
  • \- Not signed an informed consent.

结局指标

主要结局

未指定

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