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临床试验/DRKS00005587
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MotionTherapy@Home - baseline study for evaluation of safety and efficacy of a robotic locomotion training device for therapy at home - MotionTherapy@Home

Stiftung Orthopädische Universitätsklinik; Abteilung Orthopädie II0 个研究点目标入组 25 人开始时间: 2013年12月6日最近更新:
适应症

试验速览

阶段
未知
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
Interventional
分配方式
N/a: Single Arm Study
盲法
Open (masking not used)

入排标准

年龄范围
18 Years 至 60 Years(—)
性别
All

入选标准

  • motor incomplete spinal cord injury; time after trauma between 1 and 5 years; age between 18 and 60; traumatic, haemorrhagic spinal cord injury or spinal cord injury after disc herniation; Walking Index for Spinal Cord Injury >= 5 (basic walking function)

排除标准

  • body weight > 130kg; body height > 200cm; leg length discrepancy > 2 cm; moderate to severe contractures of hip, knee and ankle joints (> 20% of the normal range of motion); severe osteoporosis in the legs; instable fractures, open injuries or pressure sores at the trunk or lower extremities; extreme spasticity; cardiovascular, pulmonary, metabolic or additional orthopedic diseases that additionally restrict the walking function; severe depression; non-neglectable (> 15%) changes in baseline parameters (signs of neurological recovery); WISCI > 20 and one-leg stand possible for min. 3 sec bilaterally (already normal walking function)

研究者

发起方
Stiftung Orthopädische Universitätsklinik; Abteilung Orthopädie II

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