Het effect van de ruggenprik op pijn perceptie en sedatie in gezonde vrijwilligers

Recruiting

• Conditions: pain processingendogenous pain modulationsedationverwerken van pijnprikkelsendogene pijnstillingsedatie

• Registration Number: NL-OMON26547
• Lead Sponsor: MC

Brief Summary

/A

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 28 February 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: Not specified
• Target Recruitment: 16

Inclusion Criteria

Healthy male volunteers, aged 18 to 45 years, right-handed

Exclusion Criteria

-Obesity (BMI > 30);

-Significant history of any cardiac or vascular disorder, asthma or other pulmonary disease, major gastrointestinal abnormalities, peptic ulceration, hepatic, neurological, psychiatric, hematological (including bleeding disorders), endocrine, renal, or major genitourinary disease;

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
fMRI analysis, BOLD response.

Secondary Outcome Measures

Name	Time	Method
experimental heat pain, performed with the Pathway (Medoc Ltd, Ramat Yishai, Israel), a device that is able to heat a probe to a predefined temperature.