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Clinical Trials in Denmark / NCT07395882
Starting soon Not applicable

A New Model to Induce Itch and Inflammation

NCT07395882 · tracked via the Priya Life Science Denmark tracker
Phase
Not applicable
Started
2026-02-15
Last updated
2026-02-11

Condition(s) studied

Itching

Investigational drug(s) / intervention(s)

Cowhage (Mucuna Pruriens)HistamineHeat

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)

Trial sites (1)

FacilityCityRegionStatus
Center for Neuroplasticity and Pain Faculty of Medicine, Aalborg University Selma Lagerløfs Vej 249 9260 Gistrup, Denmark Aalborg Aalborg

More Aalborg University trials in Denmark

Other trials for the same condition

Official registry record

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.

View NCT07395882 on ClinicalTrials.gov ↗ ← All trials in Denmark