Scientists watch inflammation change skin and mood in real time
NCT ID NCT06618716
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at how acute inflammation changes blood flow in the skin and affects mood. Twenty-five healthy adults received either a placebo or an inflammation-triggering injection on separate days. Researchers measured skin temperature, blood flow, and psychological responses to understand why people react differently to inflammation.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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25 people
The number who actually took part.
- Started
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Sep 2024
- Finished
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Mar 2025
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 40 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Healthy * 18-40 years-old * Consent form signed * Having a Swedish personal identification number (personnummer) Exclusion Criteria: * Non-fluent in Swedish * Unable to read * Unable or unwilling to provide informed consent * BMI below 18.5 or above 25 kg/m2 * Smoking * Excessive alcohol consumption * Pregnancy or breastfeeding * Positive on drug screening * Current somatic disease including skin disease affecting the measurement areas * Current depression, anxiety, sleep disturbances or other psychiatric illnesses * Abnormal blood analyses: abnormal clinical levels in blood cell counts, hemoglobin, sodium, potassium, chloride, calcium, phosphate, creatinine, blood urea nitrogen, uric acid, glucose, aspartate aminotransferase, alanine aminotransferase, gamma-glutamyl transpeptidase, bilirubin, thromboplastin time and partial thromboplastin time * High-sensitivity C-reactive protein \> 10 mg/L. * History of cardiovascular, pneumological, immune disease * Moderate viral or bacterial infection in the past two weeks * Severe and/or long-term COVID-19: positive SARS-CoV-2 PCR-test or antigen-test and/or history of symptoms since February 2020 indicative of infection with SARS-CoV-2 (fever, cough, sore throat, runny or blocked nose, nausea, muscle pain, shortness of breath), which was of high intensity and/or of long duration (≥ 8 weeks). * Recent vaccination (within previous two weeks) * Abnormal cardiovascular measurements * Current or previous cancer * Any concomitant medication other than contraceptives (14 days prior to the start and throughout the study period) * Shift work or irregular sleep-wake cycle (within 14 days of the study period) * Needle anxiety or blood phobia * Invisible veins in the antecubital area of the arms or very difficult blood sampling (self-reported or experienced during screening). * Previous participation in a study involving administration of LPS
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Department of emergency medicine, Linköping University Hospital, Region Östergötland
Linköping, Sweden
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