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Clinical Trials/EUCTR2018-001371-20-FR
EUCTR2018-001371-20-FR
Active, not recruiting
Phase 1

Study of the role of local treatments on the modulation of the microbiome in psoriatic skin - Microbiome & Psoriasis Study

CHU de Nice0 sites30 target enrollmentApril 11, 2018

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Not specified
Sponsor
CHU de Nice
Enrollment
30
Status
Active, not recruiting
Last Updated
7 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
April 11, 2018
End Date
TBD
Last Updated
7 years ago
Study Type
Interventional clinical trial of medicinal product

Investigators

Eligibility Criteria

Inclusion Criteria

  • 1\. Patients of both more than 18\-year\-old sexes having signed and dated a form of information and informed consent.
  • 2\. Subject presenting a psoriasis vulgaris with symmetric hurts in size and in severity, located on elbows and\\or knees and having a score of severity (PASI)\< 10\. The hurts will have to have a surface of at least 4 cms ².
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1\.2 Adults (18\-64 years) yes
  • F.1\.2\.1 Number of subjects for this age range 28
  • F.1\.3 Elderly (\>\=65 years) yes
  • F.1\.3\.1 Number of subjects for this age range 2

Exclusion Criteria

  • 1\. Subject presenting a psoriasis in drop(gout), érythrodermique, exfoliatif or pustuleux.
  • 2\. Feminine Subject pregnant or breast\-feeding.
  • 3\. Subject having received a systematic treatment(processing) and having a potential action(share) on the psoriasis vulgaris (ex: phototherapy, cyclosporine, méthotrexate, biotherapics, steroids, or other immunosuppresseurs treatments(processings)) in 2 months preceding the randomization and during all the duration the study.
  • 4\. Subject having received a treatment(processing) antibiotic in the previous three months the visit of inclusion
  • 5\. Subject having received the topical treatments(processings) (example: corticostéroïdes, tazarotène, analogues of the vitamin D) or neutral emollients in 4 weeks preceding the randomization

Outcomes

Primary Outcomes

Not specified

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