Cowhage (Mucuna Pruriens): The spicules will be manually inserted. Approximately 30-35 spicules are gently rubbed into a 1 cm diameter skin area on the forearm/face
Histamine: To deliver histamine, standard allergy skin prick test (SPT) lancets are applied
Heat: 45 °C x 5 min
Study summary
This project aims to create a reliable, long-lasting itch model by synergistically combining thermal pre-conditioning with the application of histamine or cowhage.
Eligibility
Sex
ALL
Min age
18 Years
Max age
60 Years
Healthy volunteers
Accepted
Inclusion Criteria:
* Healthy men and women
* 18-60 years
* Speak and understand English
Exclusion Criteria:
* Pregnancy or lactation
* Drug addiction defined as any use of cannabis, opioids, or other addictive drugs
* Previous or current history of neurological (e.g., neuropathy), immunological (e.g., asthma, immune deficiencies, arthritis), musculoskeletal (e.g., muscular pain in the upper extremities), cardiac disorder (e.g., stroke), or psychiatric diagnoses (e.g., depression, bipolar disorders, acute and chronic psychosis) that may affect the results
* Current use of medications that may affect the trial, such as antihistamines, antipsychotics, painkillers, and systemic or topical steroids
* Skin diseases (e.g., atopic dermatitis, pruritus nodularis, eczema, psoriasis)
* Moles, scars, or tattoos in the area to be treated or tested (forearm/hand).
* Consumption of alcohol or painkillers 24 hours before the study days and between these
* Acute or chronic pain
* Unable to answer the "Transcranial Magnetic Stimulation Adult Safety Screen" (subprojects 2-4)
* Contraindications to transcranial magnetic stimulation (TMS) application (history of epilepsy, metal implants in head or jaw, etc.) (subprojects 2-4)
* Presence of implanted hearing aids or metal implants on the face, including permanent makeup or tattoos (subprojects 2-4)
* Contraindications to capsaicin, including intolerance to chili or burns or wounds at the application sites (subprojects 2, 3, and 4)
* Participation in other trials within one week of study entry (four weeks in the case of pharmaceutical trials)
* The subject is assessed as unable to engage in the necessary cooperation required by the study
Primary outcome measure(s)
Measuring pain by computerized Visual Analog Scale Scoring — Day 1 We will ask the subjects to rate the sensation of pain on a 100
Measuring Itch by computerized Visual Analog Scale Scoring — Day 1 We will ask the subjects to rate the sensation of itch on a 100
Measuring pain by computerized Visual Analog Scale Scoring — Day 2 We will ask the subjects to rate the sensation of pain on a 100
Measuring Itch by computerized Visual Analog Scale Scoring — Day 2 We will ask the subjects to rate the sensation of itch on a 100
Trial sites (1)
Facility
City
Region
Status
Center for Neuroplasticity and Pain Faculty of Medicine, Aalborg University Selma Lagerløfs Vej 249 9260 Gistrup, Denmark
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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