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临床试验/NCT04621747
NCT04621747Unknown不适用

Trial Investigating the Characteristics of Knismesis - a Lever to Explore Allodynia in Neuropathic Pain

University Hospital, Clermont-Ferrand2 个研究点 分布在 1 个国家目标入组 24 人开始时间: 2021年11月23日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
24
试验地点
2
主要终点
Intensity of annoying sensation

研究概览

简要总结

Also known as a "moving itch", knismesis is a mildly annoying sensation caused by a light movement on the skin, such as from a crawling insect. Its underlying mechanism rely on spatial summation, i.e. amplification of the signal due to summation of stimulated fields, like it is for dynamic allodynia in neuropathic pain. This physiological study aims at determining the physical factors of the cutaneous stimulation inducing knismesis as well as the effect of confounding factors. The main area of exploration will be the back, because of its size and the possibility to blind the participant. The information collected, along with animal data in surrogate models, would help to better understand neuropathic pain in the future.

详细描述

This is a physiological proof-of-concept, also aiming to validate a functional exploration model in healthy volunteers. Each participant will undergo a battery if psychometric then psychophysics tests, presented sequentially. However, most of the main study tests (knismesis) will be admistered in a random order (crossover). The primary endpoint is to characterise, in the healthy human, the physical determinants of the cutaneous stimulation inducing knismesis: length of the pathway, speed, direction, intensity, continuity break of the contact, hairiness, body site, or distraction by other cutaneous stimuli. The secondary endpoint is to study the relationship between the individual sensitivity to spatial summation (knismesis) and other individual sensitivities or profiles.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Basic Science
盲法
None

入排标准

年龄范围
18 Years 至 50 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Ability to answer French questionnaires.
  • · BMI between 19 and 30 kg/m2 at inclusion.

排除标准

  • Pregnancy or breastfeeding.
  • Natural intolerance to tickling.
  • Any cutaneous, ocular or neurological disease contraindicating the psychophysical tests.
  • Any disease or medical history that could expose the subject to unacceptable risk during the study.
  • Any medication intake within 7 days before testing.
  • History of drug or alcohol abuse.
  • Involvement in another concomitant research protocol.
  • Major dorsal hairiness.
  • Inability to undergo the tests.
  • Legal protection.
  • Concomitant involvement in another clinical research.
  • Refusal to participate.

结局指标

主要结局

Intensity of annoying sensation

时间窗: Day 8

After training, the annoying sensation is expressed by the subject through a handgrip dynamometer (Biopac systems). The signal will be treated and converted into area-under-curve response (Dualé C et al., Reg Anesth Pain Med 2011; 36:110-115).

次要结局

  • Muscular aversive response.(Day 1, Day 8)

研究者

发起方
University Hospital, Clermont-Ferrand
申办方类型
Other
责任方
Sponsor

研究点 (2)

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