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WithdrawnNCT06021405RENBOEKUpdated Mar 17, 2026

Koebner's Phenomenon in Psoriasis and Lichen Planus

An interventional study of Tape stripping in Kobner Phenomenon, Psoriasis and Lichen Planus, sponsored by Marie-Charlotte Brüggen. Withdrawn. Open to participants aged 18 Years to 70 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-03-17.

Sponsored by Marie-Charlotte Brüggen · Not applicable, Interventional, and Basic science

Why this study was withdrawn
due to personnel and financial restrictions, the study could not be conducted
Phase
Not applicable
Study type
Interventional
Enrollment
0
Allocation
Not applicable
Ages
18 Years to 70 Years
Sex
All
01

Study summary

Psoriasis and lichen planus often occur at mechanically irritated skin sites (e.g. tight clothing). The investigators would like to investigate this phenomenon in more detail in this study. For this purpose, the skin is specifically irritated at a small and cosmetically favorable site by tearing off scotch tape or rubbing with a wooden spatula. In order to be able to examine the inflammatory processes caused by the irritation more closely, a small skin sample and a skin swab are taken from the irritated area. This skin sample and the swab are repeated after three and fourteen days.

02

Conditions studied

  • Kobner Phenomenon
  • Psoriasis
  • Lichen Planus
03

In context

Psoriasis

2,028 studies on the registry are indexed under Psoriasis; 275 are open to participants now.

Browse Psoriasis studies →

Lead sponsor

This is the only study on the registry with Marie-Charlotte Brüggen as lead sponsor.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Dermatologist diagnosed psoriasis (group psoriasis), lichen planus (group lichen planus) or no skin disease (group healthy controls)
  • Subject is capable of giving
  • Signed informed consent

Exclusion criteria

Exclusion Criteria:

  • Use of systemic /immunmodulating agents in the last three months
  • Use of topical anti-inflammatory treatment in the last 7 days in the area of sampling.
  • Phototherapy in the last 4 weeks
  • Active or recurrent serious bacterial, fungal or viral infection at the time of enrollment by patient history, including patients with (HIV) infection, and infection, active or untreated latent tuberculosis.
  • Female patients of who are pregnant or breast feeding or planning a pregnancy during the duration of the trial and/or not practicing acceptable for the duration of the trial
  • Known or suspected non-compliance, drug or alcohol abuse,
  • Inability to follow the procedures of the study, e.g. due to language problems, psychological disorders, dementia, etc. of the participant,
  • Previous enrolment into the current study,
  • Enrolment of the investigator, his/her family members, employees and other dependent persons.
Terms in these criteria, in plain language(7)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

Immunosuppression

A weakened immune system. It can come from an illness, such as HIV or some blood cancers, or from medicines that turn the immune system down, for example after an organ transplant or for an autoimmune disease; steroids at higher doses count.

Read whether the line is about a condition or about medicines, and which medicines and doses it means.

HIV

The human immunodeficiency virus, which weakens the immune system.

Many studies now accept people whose HIV is controlled on treatment, judged by the viral load and the CD4 count. Check the limits this study sets.

Hepatitis B tests

Hepatitis B is a virus that infects the liver. These are separate tests: HBsAg positive usually means a current infection (a recent vaccination can briefly cause it too); total anti-HBc (HBcAb) positive means an infection now or in the past; HBV DNA measures how much virus is in the blood.

Some studies accept a past infection if HBV DNA is undetectable, sometimes with antiviral medicine during the study. Check what this study allows.

Hepatitis C tests

Hepatitis C is a virus that infects the liver. An HCV antibody test can stay positive after an infection has cleared (and is occasionally positive without one); an HCV RNA test shows whether the virus is there now.

After treatment, hepatitis C counts as cured when HCV RNA is still undetectable 12 weeks or more after the treatment ended. Studies often accept people cured this way.

Childbearing potential

Able to become pregnant: from the first period until menopause, unless permanently unable to through surgery (removal of the womb, or of both ovaries or both fallopian tubes).

Criteria for people of childbearing potential usually ask for a negative pregnancy test and for contraception during the study and for a time after it.

Contraception

Ways of preventing pregnancy. “Highly effective” methods fail less than 1% of the time a year when used correctly — for example an IUD or an implant.

Criteria usually say which methods count and how long to keep using them after the last dose, sometimes for male participants too. Some studies accept a partner’s vasectomy if it was confirmed successful and that person is the participant’s only sexual partner.

05

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
0 participants (actual)

Study arms

  • Experimental
    Tape stripping

    Procedure: Tape stripping

Interventions

  • ProcedureTape stripping

    a small area of skin will be tape-stripped with adhesive tape for up to 40 times and/or rubbed with a wooden spatula until the skin shows a slight erythema

06

What researchers measure

Primary outcomes

  1. Differences in the transcriptomic profile comparing psoriasis patients with and without induced koebner phenomenon

    Transcriptomic profile at all timepoints (reads per 55µm diameter dot)

    Time frame: Day 0, Day 3 (optional), Day 14 (optional)

Secondary outcomes

  1. Differences in the proteomic profile comparing psoriasis patients with and without induced koebner phenomenon

    Olink multiplex proteomics analysis at all timepoints

    Time frame: Day 0, Day 3 (optional), Day 14 (optional)

  2. Characterization of involved immune cells in the skin comparing psoriasis patients with and without induced koebner phenomenon

    Imaging mass cytometry (skin biopsies) at all timepoints

    Time frame: Day 0, Day 3 (optional), Day 14 (optional)

  3. Characterization of skin mikrobiome

    Skin swabs at all timepoints, analyzed by isolation and sequencing of the microbial DNA

    Time frame: Day 0, Day 3, Day 14

07

Study locations

No study locations are listed for this record.

08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from Sep 2025 to primary completion in Sep 2025, 0 months.

How these figures are worked out, and which studies are left out of them.

Registered
Aug 11, 2023
First posted
Sep 1, 2023
StartActual
Sep 1, 2025
Primary completionActual
Sep 20, 2025
CompletionActual
Sep 20, 2025
Last update
Mar 17, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Mar 17, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06021405
Lead sponsor
Marie-Charlotte Brüggen
Responsible party
Marie-Charlotte Brüggen (Prof. Dr. med. PhD, University of Zurich) — Sponsor-investigator
First posted
Sep 1, 2023
Start date
Sep 1, 2025
Primary completion
Sep 20, 2025
Completion
Sep 20, 2025
Last update
Mar 17, 2026

Study contacts

Marie-Charlotte Brüggen, MD PhD
principal investigator · University of Zurich

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is withdrawn, as verified in Mar 2025. You cannot join it, but the record below documents what was studied.

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