Actively Recruiting

Phase Not Applicable
Age: 18Years - 60Years
All Genders
Healthy Volunteers
ID07247695

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

Led by Aalborg University · Updated on 2025-12-04

30

Participants Needed

1

Research Sites

104 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are investigating how the placebo effect influences itch and pain sensations, particularly those caused by histaminergic and non-histaminergic triggers. This study includes healthy adults aged 18 to 60 and examines the relationship between these sensations and personality traits like depression, anxiety, and stress. The research is conducted by Aalborg University and focuses on understanding neuromodulation mechanisms involving pain and itch perception. During the approximately 1.5-hour experimental session, participants complete questionnaires about their perceptions of itch and pain, along with assessments of personality traits. Four areas on the volar forearms are treated with a placebo cream for 20 minutes to test the placebo effect. Afterward, two areas are randomly exposed to histamine using allergy skin prick test lancets, while cowhage spicules are applied to the other two areas. Itch and pain levels are continuously monitored for 10 minutes using a Visual Analog Scale. Participants are involved in one study session where they fill out several baseline questionnaires related to pain and itch catastrophizing, emotional regulation, and personality. During and immediately after the application of creams and pruritogens, pain and itch are measured using computerized Visual Analog Scales. The study monitors responses to assess neuromodulation effects without any masking or blinding. The entire participation includes baseline assessments and immediate measurements following interventions within a single visit.

CONDITIONS

Brief Title

Mechanisms Underlying the Placebo Effect in Both Histaminergic and Non-histaminergic Itch

Who Can Participate

Age: 18Years - 60Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Healthy men and women
  • Aged 18 to 60 years
  • Speak and understand English
Not Eligible

You will not qualify if you...

  • Pregnancy or lactation
  • Drug addiction including cannabis, opioids, or other drugs
  • History of neurological, immunological, musculoskeletal, cardiac, or psychiatric disorders affecting results
  • Presence of moles, wounds, scars, or tattoos in the treatment area
  • Current use of antihistamines or painkillers
  • Skin diseases
  • Alcohol or painkiller consumption within 24 hours before and during study days
  • Acute or chronic pain and itch
  • Participation in other trials within 1 week (4 weeks for pharmaceutical studies)
  • Contraindications to capsaicin or intolerance to chili
  • Inability to cooperate with study procedures

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Intervention

Duration - Single session

Participants receive a placebo cream applied on the volar forearm for 20 minutes. Histamine and cowhage itch stimuli are applied to study pain and itch responses.

1 visit (in-person)

Trial Site Locations

Total: 1 location

1

Aalborg University

Gistrup, Denmark, 9260

Actively Recruiting

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Research Team

S

Silvia Lo Vecchio

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

BASIC_SCIENCE

Number of Arms

1

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