Bergmannsheil, department for pain management
Bochum, North Rhine-Westphalia, 44789, Germany
NCT Number: NCT01618604
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.
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Notify Me18 year and older
All sexes
Observational
Bochum, North Rhine-Westphalia, 44789, Germany
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.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
following the standardized protocol of DFNS
Other names: QST
test stimulus by hot thermode conditioned stimulus by cold water bath
Other names: CPM, DNIC, Diffuse Noxious Inhibitory Controls
Other names: WDT, CDT, MDT, MPT, Quantitative Sensory Testing
Ruhr University of Bochum
Other
Quantitative Sensory Testing in Context With Conditioned Pain Modulation (CPM)
Acronym: CPM
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