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临床试验/NCT03763708
NCT03763708终止不适用

Spinal Cord Stimulation Research Study

MedtronicNeuro18 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2018年12月12日最近更新:
适应症

试验速览

阶段
不适用
状态
终止
入组人数
100
试验地点
18
主要终点
Numeric Pain Rating Scale (NPRS) - Cohort 1

研究概览

简要总结

To characterize the effects of stimulation parameters on pain relief and other cohort specific outcomes.

详细描述

This post market study will measure the following:

  • Numeric Pain Rating Scale
  • Satisfaction and Stimulation Assessment
  • Stimulation feedback
  • Stimulation parameters
  • Anatomical locations of active contacts
  • Stimulation thresholds
  • Location of paresthesia
  • Oswestry Disability Index
  • European Quality of Life 5-Dimensions
  • To characterize non-invasive health monitoring data

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

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

入选标准

  • 22 years of age or older
  • Implanted with a Medtronic rechargeable neurostimulation system, for a labeled indication, for at least 1 month and expected longevity of neurostimulator is at least 5 months
  • Willing and able to provide signed and dated informed consent
  • Capable of comprehending and consenting in English
  • Willing and able to comply with all study procedures, including diary completion, and visits
  • Able to differentiate between pain associated with the indication for SCS implant and other types of pain

排除标准

  • Implanted with neurostimulation system for an off-label indication
  • Currently enrolled or planning to enroll in an interventional clinical study that could potentially confound the study results
  • If female, pregnant or is of child-bearing potential and unwilling to use a medically acceptable form of birth control during the study
  • Has untreated major psychiatric comorbidity
  • Has a non-rechargeable neurostimulator where the battery longevity is not able to be estimated with the battery longevity calculator

结局指标

主要结局

Numeric Pain Rating Scale (NPRS) - Cohort 1

时间窗: Up to 5 months

To characterize the effect of different programmed settings on pain relief. The NPRS will be recorded once or daily over a period of time, where the subjects will rate their pain on a 11-point numeric rating scale of 0 to 10, with 0 representing 'No Pain' and 10 representing 'Worst pain imaginable'. The average overall NPRS pain score prior to the scheduled visit will be used for analysis.

Numeric Pain Rating Scale (NPRS) - Cohort 2

时间窗: Up to 2 months

To characterize the effect of different programmed settings on pain relief. The NPRS will be recorded once or daily over a period of time, where the subjects will rate their pain on a 11-point numeric rating scale of 0 to 10, with 0 representing 'No Pain' and 10 representing 'Worst pain imaginable'. The average overall NPRS pain score prior to the scheduled visit will be used for analysis.

Numeric Pain Rating Scale (NPRS) - Cohort 3

时间窗: Up to 3 months

To characterize the effect of different programmed settings on pain relief. The NPRS will be recorded once or daily over a period of time, where the subjects will rate their pain on a 11-point numeric rating scale of 0 to 10, with 0 representing 'No Pain' and 10 representing 'Worst pain imaginable'. The average overall NPRS pain score prior to the scheduled visit will be used for analysis.

Numeric Pain Rating Scale (NPRS) - Cohort 4

时间窗: Up to 5 months

To characterize the effect of different programmed settings on pain relief. The NPRS will be recorded once or daily over a period of time, where the subjects will rate their pain on a 11-point numeric rating scale of 0 to 10, with 0 representing 'No Pain' and 10 representing 'Worst pain imaginable'. The average overall NPRS pain score prior to the scheduled visit will be used for analysis.

Numeric Pain Rating Scale - Cohort 5

时间窗: Up to 5 months

To characterize the effect of different programmed settings on pain relief. The NPRS will be recorded once or daily over a period of time, where the subjects will rate their pain on a 11-point numeric rating scale of 0 to 10, with 0 representing 'No Pain' and 10 representing 'Worst pain imaginable'. The average overall NPRS pain score prior to the scheduled visit will be used for analysis.

Numeric Pain Rating Scale (NPRS) - Cohort 6

时间窗: Up to 7 months

To characterize the effect of different programmed settings on pain relief. The NPRS will be recorded once or daily over a period of time, where the subjects will rate their pain on a 11-point numeric rating scale of 0 to 10, with 0 representing 'No Pain' and 10 representing 'Worst pain imaginable'. The average overall NPRS pain score prior to the scheduled visit will be used for analysis.

Numeric Pain Rating Scale (NPRS) - Cohort 7

时间窗: Up to 8 months

To characterize the effect of different programmed settings on pain relief. The NPRS will be recorded once or daily over a period of time, where the subjects will rate their pain on a 11-point numeric rating scale of 0 to 10, with 0 representing 'No Pain' and 10 representing 'Worst pain imaginable'. The average overall NPRS pain score prior to the scheduled visit will be used for analysis.

Numeric Pain Rating Scale (NPRS) - Cohort 8

时间窗: Up to 0.5 months

To characterize the effect of different programmed settings on pain relief. The NPRS will be recorded once or daily over a period of time, where the subjects will rate their pain on a 11-point numeric rating scale of 0 to 10, with 0 representing 'No Pain' and 10 representing 'Worst pain imaginable'. The average overall NPRS pain score prior to the scheduled visit will be used for analysis.

Numeric Pain Rating Scale at Enrollment (NPRS) - Cohort 9

时间窗: Up to 1 month

To characterize the effect of different programmed settings on pain relief. The NPRS will be recorded once or daily over a period of time, where the subjects will rate their pain on a 11-point numeric rating scale of 0 to 10, with 0 representing 'No Pain' and 10 representing 'Worst pain imaginable'. The average overall NPRS pain score prior to the scheduled visit will be used for analysis.

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (18)

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