NL-OMON45809已完成不适用
Wearable motion sensor(s) to measure change of physical function in patients after total knee replacement. - Wearable sensor for rehabilitation
Imec Nederland0 个研究点目标入组 25 人开始时间: 待定最近更新:
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 25
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 18 至 99（—）
入选标准
- •- patient with knee osteoarthritis undergoing primary total knee replacement of one knee within 3 months.
- •- age > 18 years
- •- informed consent
- •- willing to travel to hospital for 3 additional visits
排除标准
- •a) Subjects with an artificial joint/limb in the lower body.
- •b) Subjects diagnosed with and/or taking medication for any musculoskeletal, neurological disorder or inflammatory arthritis.
- •c) Subjects who are pregnant or likely to become pregnant
- •d) Subject with known allergy to adhesive Ag/AgCl electrodes
- •e) Subjects using medication with phototoxic side effects: Tetracylines, Doxycycline, Phenothiazines, Dacarbazine, Ketoprofen, Lomefloxacin. In order to exclude possible local skin irritation from prolonged irradiation by LED-light (from activity monitor).
- •f) Patients that do not want to be informed in case of incidental findings.
研究者
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