endogene pijnstilling healthy volunteers pain measurements
Conditions
Interventions
Pain measurements
Sponsors
Leids Universitair Medisch Centrum
Eligibility
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: Healthy volunteers, aged 18 to 35 years, right-handed.
Exclusion criteria
Exclusion criteria: - Unable to understand study information or give oral and written informed consent; - Obesity (BMI > 30 kg/m2); - History of chronic alcohol or illicit drug use; - History of illness, condition or medication use that, in the opinion of the investigator, might interfere with optimal participation, or could confound the results of the study; - Pregnancy / lactation
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The aim of this study is to assess the usefulness of the Q-sense CPM device for CPM studies. The end-point is defined as: reproducible and significant pain relief of the test stimulus when combined with the appropriate conditioning stimulus. | — |
Secondary
| Measure | Time frame |
|---|---|
| Furthermore, we will evaluate whether the anatomic site used will impact the measured CPM effect. | — |
Countries
Netherlands
Outcome results
None listed