NCT04537468

Brief Summary

The purpose of this study was to develop a non-invasive method to measure mRNA levels using tape stripping on the skin of patients with psoriasis and patients with atopic dermatitis.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
61

participants targeted

Target at P50-P75 for not_applicable healthy

Timeline
Completed

Started May 2017

Longer than P75 for not_applicable healthy

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

May 11, 2017

Completed
2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 22, 2019

Completed
4 months until next milestone

Study Completion

Last participant's last visit for all outcomes

October 2, 2019

Completed
11 months until next milestone

First Submitted

Initial submission to the registry

August 28, 2020

Completed
6 days until next milestone

First Posted

Study publicly available on registry

September 3, 2020

Completed
Last Updated

September 4, 2020

Status Verified

September 1, 2020

Enrollment Period

2 years

First QC Date

August 28, 2020

Last Update Submit

September 2, 2020

Conditions

Keywords

Skin squamesTape strippingSkin biopsy

Outcome Measures

Primary Outcomes (1)

  • Expression of skin biomarkers

    Gene expression of epidermal cytokines and chemokines.

    Day 0

Study Arms (1)

Skin sample collection

OTHER

Skin sample collection for gene expression analyses.

Other: Skin squame collectionOther: Tape strip collectionOther: Tape strip and skin biopsy collection

Interventions

Subjects underwent skin squame collection by scraping. The investigator gently scraped the surface of a lesional skin area for patients with psoriasis, and of a non-lesional skin area for healthy volunteers to collect superficial cells. These samples were analyzed by gene expression analyses.

Skin sample collection

The first subjects had up to 35 tape strips from a maximum of 4 areas (4 X 35 strippings) on the trunk or limbs (excluding the genital area). Patients with atopic dermatitis or psoriasis had tape stripping performed on lesional skin areas and the control subjects had tape stripping performed on nonlesional skin areas. The next subjects were used to determine the optimal number of tape strips required to obtain a good signal by gene expression analyses.

Skin sample collection

Subjects had tape stripping on up to 3 different skin areas (2 areas on lesional skin and one area of nonlesional skin for patients with atopic dermatitis or psoriasis, and 2 areas of healthy skin for control subjects) using the optimal number of tape strips, as determined in the previous part. One 4-mm skin biopsy on a tape stripped area plus one 4-mm biopsy on non-tape-stripped skin (2 biopsies per subject) were also collected.

Skin sample collection

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Subject, male or female, aged 18 years or older at the time of consent.
  • Female subjects of childbearing potential had a negative urine pregnancy test at the screening visit.
  • Subjects had to be able and willing to provide written informed consent and comply with the requirements of the study protocol. Consent was obtained prior to any study-related procedures.
  • Patient had a history of atopic dermatitis or psoriasis.
  • Patient with psoriasis had a Physician's Global Assessment (PGA) score of ≥2 at Day 0.
  • Patients with atopic dermatitis had an Investigator's Global Assessment (IGA) score of ≥2 at Day 0.

You may not qualify if:

  • Female subject was pregnant or breastfeeding.
  • Subject was participating in a clinical trial with an experimental drug or device or had participated in a clinical trial with an experimental drug or device within the last 4 weeks of the collection day (Day 0).
  • Subject was known to have hepatitis B or hepatitis C viral infection.
  • Subject was known to have immune deficiency or was immunocompromised.
  • Subject had used systemic medication, medical devices, UVB or PUVA therapy or natural health products to treat atopic dermatitis or psoriasis on the areas to be biopsied or tape stripped within 4 weeks of the collection day (Day 0).
  • Subject had used oral, intravenous steroids, or immunosuppressive medication within 4 weeks of the collection day (Day 0). Subject had used intramuscular or intra-lesional or intra-articular steroids or immunosuppressive medication on the areas to be biopsied or tape stripped within 4 weeks of the collection day (Day 0).
  • Subject had used a biologic within 12 weeks or 5 half-lives of the collection day (Day 0), whichever was longer.
  • Subject had used topical medication, natural health products or medical devices to treat atopic dermatitis or psoriasis on the areas to be tape stripped or biopsied within 2 weeks of the collection day (Day 0).
  • \*Only for subjects who underwent skin biopsy:
  • Subject had a known hypersensitivity/allergy to lidocaine.
  • Subject had a history of hypertrophic scarring or keloid formation in scars or suture sites.
  • Subject was taking anti-coagulant medication (e.g. heparin, low molecular weight \[LMW\]-heparin, warfarin, anti-platelets \[nonsteroidal anti-inflammatory drugs (NSAIDs) and low-dose aspirin (equal or lower than 81 mg) were not considered anti-platelets\]) or had a contraindication to skin biopsies.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Innovaderm Research, Inc.

Montreal, Quebec, H2X 2V1, Canada

Location

Related Publications (1)

  • He H, Bissonnette R, Wu J, Diaz A, Saint-Cyr Proulx E, Maari C, Jack C, Louis M, Estrada Y, Krueger JG, Zhang N, Pavel AB, Guttman-Yassky E. Tape strips detect distinct immune and barrier profiles in atopic dermatitis and psoriasis. J Allergy Clin Immunol. 2021 Jan;147(1):199-212. doi: 10.1016/j.jaci.2020.05.048. Epub 2020 Jul 21.

MeSH Terms

Conditions

Psoriasis

Condition Hierarchy (Ancestors)

Skin Diseases, PapulosquamousSkin DiseasesSkin and Connective Tissue Diseases

Study Officials

  • Robert Bissonnette, MD

    Innovaderm Research Inc.

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
OTHER
Intervention Model
SEQUENTIAL
Model Details: The study consisted of 3 sequential groups: 1. Collection of skin squames by scraping. 2. Collection of tape strip samples. 3. Collection of tape strip samples and skin biopsies.
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

August 28, 2020

First Posted

September 3, 2020

Study Start

May 11, 2017

Primary Completion

May 22, 2019

Study Completion

October 2, 2019

Last Updated

September 4, 2020

Record last verified: 2020-09

Data Sharing

IPD Sharing
Will not share

Locations