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临床试验/NCT05852379
NCT05852379尚未招募不适用

Transcutaneous Auricular Vagus Nerve Stimulation Paired With Rehabilitation and Pelvic Nerves Stimulation for Improvement Motor Functions of Lower Extremities in Peoples With Chronic Spinal Cord Injury

Possover International Medical Center AG0 个研究点目标入组 10 人开始时间: 2023年7月1日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
10
主要终点
Evolution of the Walking Index for Spinal Cord Injury (WISCI II

研究概览

简要总结

This study is a single blinded prospective randomized monocentric study examining the effectiveness of transcutaneous auricular vagus nerve stimulation paired with rehabilitation and low frequency/antidromic stimulation of the pelvic somatic nerves. The investigator hypothesize that treatment using transcutaneous auricular vagus nerve stimulation will improve gait recovery in spinal cord injured participants already treating by rehabilitation and pelvic nerves neuromodulation.

详细描述

In this single-blinded prospective randomized study, 10 participants (adults above 18years) with chronic spinal cord injury already managed with active rehabilitation and continuous pelvic nerves stimulation (low-frequency, antidormic) will be randomly assigned in a 1:1 ratio to active taVNS (twice daily, 30 minutes each time), or control with daily sessions of sham taVNS (0.0 mA). Rehabilitation is performed unspecifically by home-rehabilitation's team or physiotherapeutists with exercises adjusted to the participant's functional level. This protocol comprised 15 to 20 weekly hours of multidisciplinary care, including neurofunctional physiotherapy and aquatic therapy, cardiorespiratory physiotherapy (two hours/week). All participants have undergone previously an implantation of a stimulator for chronic neuromodulation of the pelvic somatic nerves according with the LION procedure. Participants and therapeutists will maintain blinding until the completion of the study (6 months). Assessment of gait function, motor symptoms are performed three time, at baseline, at 3-months follow up and at 6months follow up.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Triple (Participant, Care Provider, Outcomes Assessor)

盲法说明

Triple (participants, Care provider, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • A diagnosis of traumatic complete/incomplete apar/teraplgia
  • At least 12 months post-traumatic SCI
  • Patient included in rehabilitation program
  • After laparoscopic implantation of neurosprothesis to the pelvic nerves (LION procedure)
  • Mini-mental State examination score>24
  • Stable medication
  • Patient who voluntarily accept the test and sign an informed consent form

排除标准

  • There is a clear history of cerebrovascular stroke, and there are clear symptoms or signs of neurological deficit at the time of onset, and there are corresponding responsible lesions left on neuroimaging
  • Patients with significant visual impairment or coexisting local or systemic diseases (eg osteoarthritis, or neuro,ogical conditions) likely to affect gait are excluded from the study
  • Pathologies of the articulation and ligaments of the LE that make standing/walking anatomically impossible
  • Patients who underwent deep brain stimulation surgery or those with an implanted cardiac pacemaker are excluded
  • Those with history of alcoholism, or drug addiction, or neurological diseases that can cause cognitive impairment, such as brain injury, epilepsy, encephalitis, normal intracranial pressure hydrocephalus
  • Suffering from systemic diseases that may lead to cognitive impairment (such as liver and kidney insufficiency, endocrine diseases, vitamin deficiency)
  • Suffering from cardiac conductive dysfunctions or sleep apnea syndrome
  • Participating in other drug clinical trials
  • There are contraindications to head MRI
  • Those who are deemed unsuitable to participate the trial by the investigator

结局指标

主要结局

Evolution of the Walking Index for Spinal Cord Injury (WISCI II

时间窗: 6 months

Standardized scale that classifies the individual's walking ability in 21 levels,from 0 to 20 (Table 2), from the preoperative to the 6-month assessment. (Morganti B, Scivoletto G, Ditunno P, Ditunno JF, Molinari M. Walking index for spinal cord injury (WISCI): criterion validation. Spinal Cord 2005;43:43-71)

次要结局

  • ASIA Lower Extremity Motor(6 months)

研究者

发起方
Possover International Medical Center AG
申办方类型
Other
责任方
Sponsor

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