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Investigation of a New Human Model for Itch

A

Aalborg University

Status

Completed

Conditions

Itch

Treatments

Other: Cowhage
Other: Histamine
Other: Papain
Other: L-menthol

Study type

Interventional

Funder types

Other

Identifiers

NCT04711044
N-20200005 (third sub-project)

Details and patient eligibility

About

This third sub-project aims to evaluate the interaction between the TRPM8 receptor and pruritus by studying the anti-pruritic effect of TPRM8-agonist L-menthol on histaminergic and non-histaminergic itch induced using three different pruritogens: histamine, cowhage and papain.

Enrollment

20 patients

Sex

All

Ages

18 to 60 years old

Volunteers

Accepts Healthy Volunteers

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, dermatological, immunological musculoskeletal, cardiac disorder or mental illnesses that may affect the results (e.g. neuropathy, muscular pain in the upper extremities, etc.).
  • Lack of ability to cooperate
  • Current use of medications that may affect the trial such as antihistamines, antipsychotics and pain killers, as well as systemic or topical steroids.
  • Skin diseases
  • Moles, scars or tattoos in the area to be treated or tested.
  • Hypersensitivity to papaya and mango fruit, cashew nuts, rubber latex
  • Consumption of alcohol or painkillers 24 hours before the study days and between these
  • Acute or chronic pain
  • Participation in other trials within 1 week of study entry (4 weeks in the case of pharmaceutical trials)

Trial design

Primary purpose

Basic Science

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

20 participants in 1 patient group

Study group
Experimental group
Treatment:
Other: L-menthol
Other: Histamine
Other: Papain
Other: Cowhage

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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