Optimization of the Conditioned Pain Modulation Protocol using the Q-sense

Completed

• Conditions: endogene pijnstilling; healthy volunteers; pain measurements

• Registration Number: NL-OMON42364
• Lead Sponsor: eids Universitair Medisch Centrum

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 23 April 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 30

Inclusion Criteria

Healthy volunteers, aged 18 to 35 years, right-handed.

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

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>The aim of this study is to assess the usefulness of the Q-sense CPM device for<br /><br>CPM studies. The end-point is defined as: reproducible and significant pain<br /><br>relief of the test stimulus when combined with the appropriate conditioning<br /><br>stimulus. </p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Furthermore, we will evaluate whether the anatomic site used will impact the<br /><br>measured CPM effect.</p><br>