ELIT: Testing Protocol to Efficiently Induce Itch

Sponsor
Aalborg University (Other)
Overall Status
Enrolling by invitation
CT.gov ID
NCT05195177
Collaborator
(none)
20
1
1
22.8
0.9

Study Details

Study Description

Brief Summary

This subproject aims to evaluate a new nerve excitability protocol to induce itch in healthy controls by electrical stimulation. Itch has many similarities with pain, and the nerve fibers that mediate the two sensations probably have the same morphological and excitability properties. The method used in this project will be the same as our research group uses for studying nociceptor fibers (PTT technique), but the focus is on the itch sensation. Since the itch fibers also terminate in the epidermis, our PTT technique should also be able to activate itch fibers, similar to pain fibers. If itch could be effectively induced by electrical stimulation, this would generate a valuable tool for studying itch in healthy controls. The sub-project takes place in 2 sessions (2 hours each).

Condition or Disease Intervention/Treatment Phase
  • Drug: Anti-histamine cream 1 hour
  • Drug: Local anesthetic cream 1 hour
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
20 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Basic Science
Official Title:
Nerve Excitability Testing Protocol to Efficiently Induce Itch
Actual Study Start Date :
Nov 25, 2021
Anticipated Primary Completion Date :
Dec 20, 2022
Anticipated Study Completion Date :
Oct 20, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Study group

Drug: Anti-histamine cream 1 hour
At the start of session 1, one area of the middle forearms of the participant will be located (4x4cm). On the area, anti-histamine cream will be applied for approximately 1 hour.

Drug: Local anesthetic cream 1 hour
At the start of session 2, one area of the middle forearms of the participant will be located (4x4cm). On the area, local anesthetic cream (2.5% lidocain/2.5 prilocaine) will be applied for approximately 1 hour.

Outcome Measures

Primary Outcome Measures

  1. Perception threshold for pulse shape 1 [This outcome measurement will be estimated during sessions one and two. The outcome measure takes approximately 5 minutes to estimate.]

    The perception threshold will be estimated for the electrical stimuli with pulse shape 1. The perception threshold is defined as the transcutaneous electrical current needed for the participant to perceive the stimulus. The electrode will be placed on the arm. The perception threshold will be estimated by the method of limits and the psi method.

  2. Perception threshold for pulse shape 2 [This outcome measurement will be estimated during sessions one and two. The outcome measure takes approximately 5 minutes to estimate.]

    The perception threshold will be estimated for the electrical stimuli with pulse shape 2. The perception threshold is defined as the transcutaneous electrical current needed for the participant to perceive the stimulus. The electrode will be placed on the arm. The perception threshold will be estimated by the method of limits and the psi method.

  3. Perception threshold for pulse shape 3 [This outcome measurement will be estimated during sessions one and two. The outcome measure takes approximately 5 minutes to estimate.]

    The perception threshold will be estimated for the electrical stimuli with pulse shape 3. The perception threshold is defined as the transcutaneous electrical current needed for the participant to perceive the stimulus. The electrode will be placed on the arm. The perception threshold will be estimated by the method of limits and the psi method.

  4. Perception threshold for pulse shape 4 [This outcome measurement will be estimated during sessions one and two. The outcome measure takes approximately 5 minutes to estimate.]

    The perception threshold will be estimated for the electrical stimuli with pulse shape 4. The perception threshold is defined as the transcutaneous electrical current needed for the participant to perceive the stimulus. The electrode will be placed on the arm. The perception threshold will be estimated by the method of limits and the psi method.

  5. Perception threshold for pulse shape 1 when antihistamine cream has been applied [This outcome measurement will be estimated during session one. The outcome measure takes approximately 5 minutes to estimate.]

    The perception threshold will be estimated for the electrical stimuli with pulse shape 1 when anti-histamine cream has been applied for approximately an hour. The perception threshold is defined as the transcutaneous electrical current needed for the participant to perceive the stimulus. The electrode will be placed on the arm. The perception threshold will be estimated by the method of limits and the psi method.

  6. Perception threshold for pulse shape 2 when anti-histamine cream has been applied [This outcome measurement will be estimated during session one. The outcome measure takes approximately 5 minutes to estimate.]

    The perception threshold will be estimated for the electrical stimuli with pulse shape 2 when anti-histamine cream has been applied for approximately an hour. The perception threshold is defined as the transcutaneous electrical current needed for the participant to perceive the stimulus. The electrode will be placed on the arm. The perception threshold will be estimated by the method of limits and the psi method.

  7. Perception threshold for pulse shape 3 when anti-histamine cream has been applied [This outcome measurement will be estimated during session one. The outcome measure takes approximately 5 minutes to estimate.]

    The perception threshold will be estimated for the electrical stimuli with pulse shape 3 when anti-histamine cream has been applied for approximately an hour. The perception threshold is defined as the transcutaneous electrical current needed for the participant to perceive the stimulus. The electrode will be placed on the arm. The perception threshold will be estimated by the method of limits and the psi method.

  8. Perception threshold for pulse shape 4 when anti-histamine cream has been applied [This outcome measurement will be estimated during session one. The outcome measure takes approximately 5 minutes to estimate.]

    The perception threshold will be estimated for the electrical stimuli with pulse shape 4 when anti-histamine cream has been applied for approximately an hour. The perception threshold is defined as the transcutaneous electrical current needed for the participant to perceive the stimulus. The electrode will be placed on the arm. The perception threshold will be estimated by the method of limits and the psi method.

  9. Perception threshold for pulse shape 1 when local anaesthetic cream has been applied [This outcome measurement will be estimated during session two. The outcome measure takes approximately 5 minutes to estimate.]

    The perception threshold will be estimated for the electrical stimuli with pulse shape 1 when local anaesthetic cream has been applied for approximately an hour. The perception threshold is defined as the transcutaneous electrical current needed for the participant to perceive the stimulus. The electrode will be placed on the arm. The perception threshold will be estimated by the method of limits and the psi method.

  10. Perception threshold for pulse shape 2 when local anaesthetic cream has been applied [This outcome measurement will be estimated during session two. The outcome measure takes approximately 5 minutes to estimate.]

    The perception threshold will be estimated for the electrical stimuli with pulse shape 2 when local anaesthetic cream has been applied for approximately an hour. The perception threshold is defined as the transcutaneous electrical current needed for the participant to perceive the stimulus. The electrode will be placed on the arm. The perception threshold will be estimated by the method of limits and the psi method.

  11. Perception threshold for pulse shape 3 when local anaesthetic cream has been applied [This outcome measurement will be estimated during session two. The outcome measure takes approximately 5 minutes to estimate.]

    The perception threshold will be estimated for the electrical stimuli with pulse shape 3 when local anaesthetic cream has been applied for approximately an hour. The perception threshold is defined as the transcutaneous electrical current needed for the participant to perceive the stimulus. The electrode will be placed on the arm. The perception threshold will be estimated by the method of limits and the psi method.

  12. Perception threshold for pulse shape 4 when local anaesthetic cream has been applied [This outcome measurement will be estimated during session two. The outcome measure takes approximately 5 minutes to estimate.]

    The perception threshold will be estimated for the electrical stimuli with pulse shape 4 when local anaesthetic cream has been applied for approximately an hour. The perception threshold is defined as the transcutaneous electrical current needed for the participant to perceive the stimulus. The electrode will be placed on the arm. The perception threshold will be estimated by the method of limits and the psi method.

  13. Sensation for pulse 1 [This outcome measurement will be estimated during sessions one and two. The outcome measure takes approximately 5 minutes to estimate.]

    The investigator will ask the participant to rate the sensation of electrical stimulation with pulse 1 for the three different conditions. The conditions are: control (not active cream), antihistamine cream, and local anesthetic cream. The scale is 0-10 for the three sensations touch, itch, and pain. Zero means no sensation, and ten is the worst pain/touch/itch imaginable.

  14. Sensation for pulse 2 [This outcome measurement will be estimated during sessions one and two. The outcome measure takes approximately 5 minutes to estimate.]

    The investigator will ask the participant to rate the sensation of electrical stimulation with pulse 2 for the three different conditions. The conditions are: control (not active cream), antihistamine cream, and local anesthetic cream. The scale is 0-10 for the three sensations touch, itch, and pain. Zero means no sensation, and ten is the worst pain/touch/itch imaginable.

  15. Sensation for pulse 3 [This outcome measurement will be estimated during sessions one and two. The outcome measure takes approximately 5 minutes to estimate.]

    The investigator will ask the participant to rate the sensation of electrical stimulation with pulse 3 for the three different conditions. The conditions are: control (not active cream), antihistamine cream, and local anesthetic cream. The scale is 0-10 for the three sensations touch, itch, and pain. Zero means no sensation, and ten is the worst pain/touch/itch imaginable.

  16. Sensation for pulse 4 [This outcome measurement will be estimated during sessions one and two. The outcome measure takes approximately 5 minutes to estimate.]

    The investigator will ask the participant to rate the sensation of electrical stimulation with pulse 4 for the three different conditions. The conditions are: control (not active cream), antihistamine cream, and local anesthetic cream. The scale is 0-10 for the three sensations touch, itch, and pain. Zero means no sensation, and ten is the worst pain/touch/itch imaginable.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:

Healthy men and women in the age 18-80 years who speak and understand

Exclusion Criteria:
  • Pregnancy or breast feeding

  • Drug addiction defined as the use of cannabis, opioids or other drugs

  • Previous and present neurologic, musculoskeletal or mental illnesses (e.g., epilepsy, neuropathy, fibromyalgia and depression)

  • Skin diseases

  • Past history of conditions possibly leading to neuropathy

  • Inability to cooperate

  • Current use of medications that may affect the study, e.g., analgesics

  • Previous traumatic experience of an electrical accident

  • Consumption of alcohol or painkillers within the last 24 hours

  • Participation in other pain studies throughout the study period

  • Patients with cardiac diseases (e.g., pacemaker).

Contacts and Locations

Locations

Site City State Country Postal Code
1 Aalborg University Aalborg Aalborg Ø Denmark 9220

Sponsors and Collaborators

  • Aalborg University

Investigators

  • Principal Investigator: Jenny Tigerholm, Aalborg University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Jenny Tigerholm, Assistant Professor, Aalborg University
ClinicalTrials.gov Identifier:
NCT05195177
Other Study ID Numbers:
  • N-2020001 4-sub-project
First Posted:
Jan 18, 2022
Last Update Posted:
Jul 26, 2022
Last Verified:
Jul 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 26, 2022