跳至主要内容
临床试验/NCT01907503
NCT01907503Unknown不适用

Adaptation of Locomotor Activity in Patients Suffering From Hip OA - Analysis of This Adaptation as a Prognostic Criterion for Future Disease Progression

Centre Hospitalier Universitaire Dijon2 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2008年2月最近更新:
适应症

试验速览

阶段
不适用
入组人数
200
试验地点
2
主要终点
locomotor activity

研究概览

简要总结

To assess the prognostic value of a characteristic evaluation of gait in persons suffering from hip OA for subsequent indications for THR.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
盲法
None

入排标准

年龄范围
45 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Men or women aged between 45 and 75 years Suffering from primary hip osteoarthritis defined according to ACR criteria who presented pain in the hip for at least one month in the preceding 3 months Radiological stage II, III or IV hip OA according to the Kellgren and Lawrence classification Patients able to understand simple instructions des packaging instructions, to give their written informed consent.

排除标准

  • Indication for THR at the time of inclusion. Pregnant or breast-feeding women Alzheimer's disease Chronic respiratory insufficiency with clinical manifestations Parkinson's disease Motor neuron disease Major musculo-skeletal disorder (other than hip OA) Severe non-stabilised diabetes Non-stabilised hypertension Hip OA inflammation flare Rapidly-destructive hip OA Radiography to evaluate structural evolution of the disease done more than 12 months previously Presence of OA in another joint, or another osteoarticular or periarticular disease of the lower limbs with, in the opinion of the patient, disability due to this other disease that is greater than the disability caused by the hip OA.
  • Spine disease causing gait disturbance (radiculalgia, lumbar canal stenosis,... with, in the opinion of the patient, disability due to this other disease that is greater than the disability caused by the hip OA.)

结局指标

主要结局

locomotor activity

时间窗: participants will be followed for the duration of hospital stay, an expected average of 2 weeks

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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