Psoriasis Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People of any sex who are admitted to the Dermatology department at the CHU of Nice hospital with moderate to severe psoriasis (measured by a skin severity score of 10 or above)
- People with a clinical diagnosis of plaque psoriasis confirmed by a dermatologist, with or without type 2 diabetes (defined by a blood sugar marker called glycated haemoglobin above 7%)
- People covered by a social security scheme
- People who have given their free and informed consent to participate
- For the control group: people without psoriasis or other inflammatory skin conditions, with or without type 2 diabetes, who have given their free and informed consent
Who may not be able to join:
- People who are under 18, unable to consent, or unwilling to give free and informed consent
- Women who are pregnant or breastfeeding
- People currently excluded from participating in other biomedical research studies
- People who have a generalised chronic inflammatory disease or another inflammatory skin condition
- People who have taken certain medications recently, including: oral corticosteroids or immune-modifying drugs in the past month, corticosteroid creams or treatments in the past 15 days, certain targeted biological therapies (anti-IL-23 or anti-IL-12/23) for less than 3 months, or other biological therapies (anti-IL-17 or anti-TNF) for less than 1 month
- People for whom a small skin biopsy (tissue sample) would be medically unsafe — for example, those with a known bleeding disorder, who take blood-thinning medications, who have an allergy to a local anaesthetic called xylocaine, who have a history of raised/keloid scarring, or who have a congenital immune deficiency
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: passeron thierry, CHU de Nice, Service de Dermatologie
Phone: +33492036488
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Percentage of dentridic cells producers of IL-23
Can't join this trial?
Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.