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Study identifier: NCT06503510 Synced from ClinicalTrials.gov · August 08, 2026
● Study status: RecruitingIL-13

Role of Interleukin-13 Pathways on Pain and Itch Sensitivity

Condition: Itch  ·  Sponsor: Aalborg University

PhaseNA
Planned participants20
Who can joinAll sexes, 18 Years to 60 Years
Healthy volunteersYesCheck eligibility criteria ↓
Where3 locations

Interested? Contact the study team ↓

Sponsor, CRO or site team? See where this study is running → — listed sites, countries and recruiting context. Everything below is written for patients and caregivers.

About this study

Atopic dermatitis (AD) is as chronic, inflammatory skin disorder affecting 20% of the world's population. Intense itch and skin pain are the main symptoms. Research has shown that the proteins interleukins are involved in inflammation and itch in atopic dermatitis. The medicinal product called Lebrikizumab, used for treatment of AD, has shown to block the interleukin called IL-13. The purpose of this experiment is to evaluate the role of IL-13 in itch in both healthy subjects and people with atopic dermatitis.

This description comes directly from the study's public registry record.

Talk to the study team

Silvia Lo Vecchio  ·  21397785  ·  slv@hst.aau.dk

There is no obligation to join — the study team can answer your questions about taking part.

Always discuss trial participation with your own doctor first.

Full eligibility criteria (exactly as the study team wrote them)

Inclusion Criteria: * Healthy men and women * 18-60 years Exclusion Criteria: * Pregnancy or lactation * Drug addiction defined as any use of cannabis, opioids, or other drugs * Previous or current history of neurological, dermatological (e.g., AD, psoriasis, etc.), immunological, musculoskeletal, cardiac disorder, or psychiatric diagnoses that may affect the results (e.g., neuropathy, muscular pain in the upper extremities, anxiety, depression, schizophrenia, etc.) * Moles, wounds, scars, or tattoos in the area to be treated or tested * Current use of medications that may affect the trial such as antihistamines and pain killers (use of antihistamines should be discontinued 72 hours before the experiment and all topical agents and emollients should be discontinued 24 hours before the experiment). * Use of systemic and topical corticosteroids * Consumption of alcohol or painkillers 24 hours before the study days and between these * Acute or chronic pain * Participation in other trials within one week of study entry (four weeks in the case of pharmaceutical trials) * Lack of ability to cooperate

Reproduced word-for-word from the public registry record — the study team can answer questions about it.

Locations (3)

Aalborg UniversityGistrup, Aalborg, DenmarkRecruiting
CNAPGistrup, Aalborg, DenmarkActive Not Recruiting
Aalborg UniversityAalborg, Denmark, DenmarkNot Yet Recruiting

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GistrupAalborg

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