Clinical trial Recruiting at 1 site Interventional Ages 18 to 60

Placebo effects on histamine and cowhage-induced itch

Official title: Pain and Itch Neuromodulation: Effects of Offset Analgesia, Placebo, and Nocebo and Topographical Distribution of Itch and Pain Receptors

Run by Aalborg University · NCT07247695 · Data updated 2026-11-12

This one-time, 1½-hour session will test whether applying a harmless cream reduces histamine- and cowhage-induced itch in healthy adults aged 18–60.

Quick facts

Study typeInterventional
Ages18 Years to 60 Years
SexAll
Enrollment30 (estimated)
SponsorAalborg University
Academic / other
Locations1 site (Gistrup)
StatusRecruiting
StartedNovember 3, 2025
Main results expectedDecember 31, 2026
Study endsDecember 31, 2028
Registry record updatedDecember 4, 2025
Trial IDNCT07247695 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Healthy English-speaking adults aged 18–60 with intact forearm skin, no chronic itch or pain, not pregnant or lactating, and not taking antihistamines or painkillers are ideal candidates.

Probably not a fit

People with chronic or active skin disease, current use of antihistamines or pain medications, pregnancy or lactation, neurological or psychiatric disorders, recent drug use, or forearm wounds/tattoos are unlikely to be eligible or to benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

Participants first complete questionnaires about how they perceive itch, pain, and mood and about personality traits. Four sites (two on each forearm) are treated with the same inert vehicle cream for 20 minutes to create a placebo context; afterward two sites are randomly challenged with histamine and two with cowhage. Itch and pain are continuously recorded on a visual analog scale during the 10-minute pruritogen application. The within-subject design in healthy volunteers compares placebo responsiveness between histaminergic and non-histaminergic itch over a single 90-minute session.

Why it matters

Potential benefit: If successful, the results could help develop non-drug approaches to reduce acute itch and guide use of placebo mechanisms in symptom management.

How similar studies have gone: Placebo effects on itch—especially histamine-induced itch—have been reported, but direct comparison of placebo responses between histaminergic and cowhage (non-histaminergic) itch is relatively novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
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 drugs
* Previous or current history of neurological, 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
* Skin diseases
* Consumption of alcohol or painkillers 24 hours before the study days and between these
* Acute or chronic pain and itch
* Participation in other trials within 1 week of study entry (4 weeks in the case of pharmaceutical studies)
* Contraindications to capsaicin, including intolerance to chili or burns or wounds at the application site
* The subject is assessed as unable to engage in the necessary cooperation required by the study

Where it's running

  • Aalborg University
    Gistrup, Denmark
    Recruiting

Study contacts

  • Principal investigator: Silvia Lo Vecchio — Aalborg Universitet
  • Study coordinator: Silvia Lo Vecchio
  • Email: slv@hst.aau.dk
  • Phone: +4521397785

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.