跳至主要内容
临床试验/NCT01618604
NCT01618604已完成不适用

Quantitative Sensory Testing in Context With Conditioned Pain Modulation (CPM)

Ruhr University of Bochum1 个研究点 分布在 1 个国家目标入组 26 人开始时间: 2012年5月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
26
试验地点
1

研究概览

简要总结

Conditioned Pain Modulation (CPM) is a phenomenon which isn't examined enough. Many factors of influence such as gender, age and psyche are already known - but the duration of such effects, their reliability and the correlation between standardized Quantitative Sensory Testing (QST) and CPM is still unknown.

In this study the investigators expect to find parameters in QST that correlate with the efficacy of Conditioned Pain Modulation. Knowing factors that indicate high or low potential CPM could help finding patients-at-risk and adapting their therapy.

详细描述

Conditioned Pain Modulation was firstly found in rats by electrical stimulation of their spinal cord and called Diffuse Noxious Inhibitory Controls. In humans such experimental settings are impossible. That is why we need two noxious stimuli for provoking such an endogenous pain inhibition.

Before the CPM setting begins, we will investigate our 32 healthy probands by basic QST following the protocol of DFNS (German Research Network on Neuropathic Pain). This assessment helps us to create a sensory profile for every proband and to look for correlations between QST parameters and CPM efficacy. Then the CPM setting follows. In our experimental design we use a test stimulus (TS) on the dominant forearm by thermode (normally 45-47°C, depending on the pain rating, we need scores >NRS 60) and a conditioned stimulus (CS) on the other hand by cold water bath (10°C). Both stimuli must be rated on the numerical rating scale (NRS) 0-100 alone and in combination. A positive effect can be seen, if the difference between TS alone and TS in combination with CS is >0. To learn more about the duration of CPM effects we decided to repeat four QST parameters (cold detection threshold, warm detection threshold, mechanical detection threshold and mechanical pain threshold) within 30 minutes after finishing the CPM part to detect changes of time.

The whole study design will be repeated 24-72h hours later to increase the test-retest-reliability.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Prospective

入排标准

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

入选标准

  • healthy probands >18 years
  • right-handedness
  • informed consent
  • no chronic pain
  • no drugs (but oral contraceptives)
  • no neurological diseases
  • no psychiatric diseases

排除标准

  • no informed consent
  • language deficits
  • left-handedness
  • not enough pain intensity by thermode or cold water bath
  • psychiatric disease, neurological diseases other chronic disease
  • chronic pain syndromes
  • pregnancy or lactation
  • permanent drug use, drug use in the last 14 days

研究者

发起方
Ruhr University of Bochum
申办方类型
Other
责任方
Principal Investigator
主要研究者

Christoph Maier, Prof. Dr.

Head of the Dep. of Pain Management

Ruhr University of Bochum

研究点 (1)

Loading locations...

相似试验

QST in Context With Conditioned Pain Modulation | 临床试验