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临床试验/JPRN-jRCTs032190053
JPRN-jRCTs032190053招募中1 期

Evaluation of safety of knee extension and flexion training using the wearable motion support robot (single joint type of Hybrid Assistive Limb (HAL-SJ)) for patients with anterior cruciate ligament injury - Evaluation of safety of knee extension and flexion training using the wearable motion support robot (single joint type of Hybrid Assistive Limb (HAL-SJ)) for patients with anterior cruciate ligament injury

Yamazaki Masashi0 个研究点目标入组 30 人开始时间: 2019年7月8日最近更新:
适应症

试验速览

阶段
1 期
状态
招募中
发起方
入组人数
30

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
>= 15age old 至 < 50age old(—)
性别
All

入选标准

  • All patients with ACL-injured patients and ACL reconstructive surgery who were consulted at our hospital orthopedic surgery
  • 1.Primary ACL injured patients
  • 2.Patients with harvested are semitendinosus tendon alone or both semitendinosus and gracilis tendons
  • 3.Be observable throughout the entire research period
  • 4.Patients who weigh 40-100 kg and height 150-190 cm and are able to wear HAL
  • 5.Patient who can accept document consent

排除标准

  • Patients who conflict with one of the following criteria are excluded and are not subject to this clinical study
  • 1.Patients with multiple knee ligament injuries
  • 2.Bilateral simultaneous surgery patient
  • 3.Patients who are considered difficult to wear and train HAL due to underlying disease or perioperative complications
  • 4.Patients with bleeding tendencies or complications that are problematic for training
  • 5.Patients who can not affix HAL biological electrode due to skin diseases or other things
  • 6.Patients who had participated in other research within 12 weeks of starting this clinical study
  • 7.Patients who judged that participation in this study is inappropriate by clinical trial responsible doctor or clinical trial sharing doctor

研究者

发起方
Yamazaki Masashi

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