跳至主要内容
临床试验/NCT04662320
NCT04662320进行中(未招募)不适用

Promoting Healing of Nerves Through Electrical Stimulation

Checkpoint Surgical Inc.10 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2021年9月1日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
100
试验地点
10
主要终点
Change in Grip Strength at 1 year.

研究概览

简要总结

This study is evaluating a new therapeutic use of electrical stimulation to promote nerve healing and improve functional recovery following surgical intervention for nerve compression. A single dose of the therapeutic stimulation is delivered as part of the surgical intervention to address compression of the ulnar nerve at the elbow.

详细描述

Preliminary research has shown that delivering a brief period of electrical stimulation following nerve repair promotes nerve healing and functional recovery. This study is investigating the use of a single dose of therapeutic electrical stimulation to promote nerve healing. The therapy is delivered as part of the surgical intervention to address compression of the ulnar nerve at the elbow, commonly referred to as Cubital Tunnel Syndrome.

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
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Electrodiagnostic evidence of ulnar neuropathy at the elbow.
  • Are candidates for surgical intervention.
  • Evidence of motor involvement such as intrinsic muscle atrophy or weakness.
  • Are age 18-80 years.
  • Signed and dated informed consent form.

排除标准

  • Severe comorbid condition, such as arrythmia or congestive heart failure, preventing surgery
  • Previous history or current transection of ulnar nerve, or concomitant upper extremity nerve injury
  • Global peripheral neuropathy affecting the hands
  • Age less than 18 or greater than 80 years
  • Un-affected hand maximum grip strength <12kg

结局指标

主要结局

Change in Grip Strength at 1 year.

时间窗: 1 year

Change in grip strength at 1 year from baseline (pre-operative) assessment.

次要结局

  • Medical Research Council (MRC) motor grading.(Pre-surgery, 6 weeks, 3 months, 5 months, 7 months, 9 months, and 1 year)
  • Patient Reported Outcome Measurement System (PROMIS) Upper Extremity Function(Pre-surgery, 10 days, 6 weeks, 3 months, 5 months, 7 months, 9 months, and 1 year)
  • Michigan Hand Questionnaire (MHQ)(Pre-surgery, 10 days, 6 weeks, 3 months, 5 months, 7 months, 9 months, and 1 year)
  • 2-point discrimination(Pre-surgery, 6 weeks, 3 months, 5 months, 7 months, 9 months, and 1 year)
  • Lateral Pinch Strength(Pre-surgery, 6 weeks, 3 months, 5 months, 7 months, 9 months, and 1 year)
  • Patient Reported Outcome Measurement System (PROMIS) Pain Interference(Pre-surgery, 10 days, 6 weeks, 3 months, 5 months, 7 months, 9 months, and 1 year)
  • Electromyography (EMG)(Pre-surgery, 3 months, and 7 months)
  • Grip Strength(Pre-surgery, 6 weeks, 3 months, 5 months, 7 months, 9 months, and 1 year)
  • Semmes-Weinstein Monofilament Testing(Pre-surgery, 6 weeks, 3 months, 5 months, 7 months, 9 months, and 1 year)
  • Maximal finger spread measurement.(Pre-surgery, 6 weeks, 3 months, 5 months, 7 months, 9 months, and 1 year)
  • Nerve Conduction Velocity (NCV)(Pre-surgery, 3 months, and 7 months)

研究者

发起方
Checkpoint Surgical Inc.
申办方类型
Industry
责任方
Sponsor

研究点 (10)

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