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Study of Molecular Markers in Cutaneous Inflammation Between Psoriatic Lesional Skin and Healthy Non-lesional Skin (EMIP)

C

Centre Hospitalier Régional d'Orléans

Status

Completed

Conditions

Psoriasis

Treatments

Procedure: Biopsy

Study type

Interventional

Funder types

Other

Identifiers

NCT03423004
CHRO-2017-12

Details and patient eligibility

About

The project topic consists on re-conciliating the fine tuners of the gene expression "microRNAs" and the immunopathogenic occasions responsible for skin disorders in context of skin infection and inflammation such as psoriasis. The skin is a network of effector cells and molecular mediators that constitute a highly sophisticated "Skin Immune System (SIS) described by Jan D Bos in 1986. The cutaneous homeostasis maintenance is dependent on the cross talk between several immune sentinels present in the different compartments of the skin as well as the interplay between innate and adaptive immune responses. The whole is under the control of gene regulation. However, cutaneous homeostasis disruption occurs when the SIS safe framework erroneously sends aggravation signals due to gene regulation disbalance via inflammatory cellular and molecular mediators into the site of infection causing chronic inflammation characterized by thick red irritated skin lesions. The latter was showed to have a characteristic microRNA (regulators of gene expression) signature.

Enrollment

9 patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Men or women between 18 and 75
  • Clinical diagnosis of chronic active psoriasis in non-pustular plaque
  • Treated locally with topical corticosteroids

Exclusion criteria

  • Patient who did not give express consent to participate
  • No affiliation to a social security scheme
  • Patient treated systemically
  • Thrombocytopenic patient
  • Patient known to be HIV-positive
  • Septic patient
  • Patient with only facial lesions
  • Patient with psoriasis with joint involvement
  • Patient participating in another study
  • Patient protected under the law (under guardianship or trusteeship)
  • Pregnant or lactating woman

Trial design

Primary purpose

Basic Science

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

9 participants in 2 patient groups

Patient with lesional skin
Experimental group
Description:
the sample will be taken by superficial cutaneous biopsy in psoriasic patients
Treatment:
Procedure: Biopsy
Patients with healthy skin
No Intervention group
Description:
the skin will be recovered during a surgical procedure (surgical waste) for patients who will not be opposed

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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