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
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.
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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