跳至主要内容
临床试验/NCT03877016
NCT03877016已完成不适用

Prospective, Multicentric, Randomized on Two Arms, Controlled, by Cross-over, Pilot Study, in Order to Evaluate Disconfort Among Outpatients Using actiTENS for Neuropathic Pain vs TENS ECO 2.

Centre Hospitalier Universitaire, Amiens5 个研究点 分布在 1 个国家目标入组 72 人开始时间: 2019年9月17日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
72
试验地点
5
主要终点
Disconfort of using TENS (Electrical Nerve Stimulation Therapy) Eco2 versus actiTENS

研究概览

简要总结

Non-pharmacological treatments for pain relief are more and more used in clinical care although any scientific validation. Among the non-pharmacological treatments of neuropathic pain relief, TENS (Electrical Nerve Stimulation Therapy) is the major treatment with the best benefit. Unfortunately, the use of TENS by patients appears very difficult. Because of this inconvenience, more than 40% of TENS users interrupt the treatment despite treatment benefit. A new TENS device: actiTENS that seems to be less constraining than TENS is now available in France. ActiTENS efficacy and safety compared to TENS need to be investigated.

The main objective is to evaluate and to compare the use of actiTENS, with TENS Eco 2, the classical device in patients with chronic neuropathic pain.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Other
盲法
None

入排标准

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

入选标准

  • •Patient covered by national health insurance
  • •Patient able to express consent
  • •Patient with neuropathic pain with DN4 (Douleur Neuropathique 4 Questions) > or = 4/
  • •Actual or potential neurologic lesion
  • •Patient still using a TENS device

排除标准

  • •Planned surgery in the next two months
  • •Modification of the reatment in the next two motnhs
  • •Other study ongoing for the patient
  • •Medical contraindication for TENS

研究组 & 干预措施

TENS Eco2

Active Comparator

TENS Eco2 is the classical device in patients with chronic neuropathic pain

干预措施: TENS (Procedure)

actiTENS

Experimental

ActiTENS is a new TENS device, that seems less cotraining.

干预措施: TENS (Procedure)

结局指标

主要结局

Disconfort of using TENS (Electrical Nerve Stimulation Therapy) Eco2 versus actiTENS

时间窗: day 35 after patient inclusion

Discomfort evaluation will be determined by using VAS (Visual Analogue Scale)

Disconfort of using TENS (Electrical Nerve Stimulation Therapy) Eco2 versus actiTENS

时间窗: day7 after patient inclusion

Discomfort evaluation will be determined by using VAS (Visual Analogue Scale)

次要结局

  • length of TENS daily use(day 35 after patient inclusion)
  • length of TENS daily use(day7 after patient inclusion)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (5)

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