跳至主要内容
临床试验/NL-OMON37488
NL-OMON37488已完成不适用

A Post Market Cohort to Assess the Performance of the Spinal Modulation Neurostimulator System for the Management of Chronic Intractable Pain - Performance of the Spinal Modulation Neurostimulator System

Spinal Modulation NV0 个研究点目标入组 80 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
80

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

  • 1.Subject is at least 18 years old
  • 2.Subject is able and willing to comply with the follow-up schedule and protocol
  • 3.Chronic, intractable pain in the thoracic, lumbar, and/or sacral distribution(s) for at least 6 months
  • 4.Failed conservative treatments for chronic pain including but not limited to pharmacological therapy, physical therapy and interventional pain procedures for chronic pain
  • 5.Minimum baseline pain rating of 60 mm on the VAS in the primary region of pain
  • 6.In the opinion of the investigator, the subject is psychologically appropriate for the implantation for an active implantable medical device
  • 7.Subject is able to provide written informed consent
  • 8.Subject speaks Dutch or English

排除标准

  • 1.Female subject of childbearing potential is pregnant/nursing, plans to become pregnant or is unwilling to use approved birth control
  • 2.Escalating or changing pain condition within the past month as evidenced by investigator examination
  • 3.Subject has had corticosteroid therapy at an intended site of stimulation within the past 30 days
  • 4.Subject has had radiofrequency treatment of an intended target DRG(s) within the past 3 months
  • 5.Subject currently has an active implantable device including ICD, pacemaker, spinal cord stimulator or intrathecal drug pump
  • 6.Subject has pain only or primarily within a cervical dermatomal distribution
  • 7.Subject is unable to operate the device
  • 8.Subjects with indwelling devices that may pose an increased risk of infection
  • 9.Subjects currently has an active infection
  • 10.Subject has, in the opinion of the investigator, a medical comorbidity that contraindicates placement of an active medical device
  • 11.Subject has participated in another clinical investigation within 30 days
  • 12.Subject has a coagulation disorder or uses anticoagulants that, in the opinion of the investigator, precludes participation
  • 13.Subject has been diagnosed with cancer in the past 2 years

研究者

发起方
Spinal Modulation NV

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