Skip to main content
OpenTrials
Completed

NCT Number: NCT01618604

QST in Context With Conditioned Pain Modulation

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.

Completed

Looking for future studies?

Notify Me

Key information

Conditions

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Bergmannsheil, department for pain management

Bochum, North Rhine-Westphalia, 44789, Germany

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

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

Exclusion criteria

  • 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

Treatment and study plan

Quantitative sensory testing

Procedure

following the standardized protocol of DFNS

Other names: QST

Conditioned Pain Modulation

Procedure

test stimulus by hot thermode conditioned stimulus by cold water bath

Other names: CPM, DNIC, Diffuse Noxious Inhibitory Controls

Repetition of four QST parameters

Procedure
  • warm detection threshold (WDT)
  • cold detection threshold (CDT)
  • mechanical detection threshold (MDT)
  • mechanical pain threshold (MPT)

Other names: WDT, CDT, MDT, MPT, Quantitative Sensory Testing

Sponsors and collaborators

Lead sponsor

Ruhr University of Bochum

Other

Registry information

Official study title

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

Acronym: CPM

Important dates

Study start
2012
Primary completion
2012
Study completion
2012
First posted
Jun 13, 2012
Registry last updated
Jan 3, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.