Deployment o the Multidisciplinary Prospective Cohort Imminent (IMMINeNT)

University Hospital, Lille

Status: Enrolling

Conditions: Atopic Dermatitis; Severe Asthma; Behçet Disease; Multiple Sclerosis; Angioedema; Systemic Sclerosis; Chronic Inflammatory Disease; Lupus; Psoriatic Arthritis

Treatments: Other: SF-12 questionnaire; Genetic: Biobanking with genetic analysis

Study type: Interventional

Funder types: Other

Identifiers

NCT04334031

2018_82

2019-A01309-48 (Other Identifier)

Details and patient eligibility

About

Immune-mediated inflammatory diseases (IMIDs) most often affect young patients and have high impact on morbidity and mortality with a significant alteration in the quality of life of patients with professional, social and emotional repercussions.

Beyond this burden, IMIDs share many common pathophysiological mechanisms and treatments, known as "targeted therapies". Despite progress in this field, much remains to be done in clinical, therapeutic and fundamental research to address the efficacy, resistance and side-effects of treatment.

These similarities between IMIDs have led the FHU IMMINeNT to propose the creation of a prospective, multidisciplinary clinical-biological database (IMMINeNT cohort), associated to a biobank, of patients with IMIDs. The main objectives of this database will be to identify new prognostic and therapeutic biomarkers in order to develop new therapeutic targets and biomarkers, to identify prognostic factors and determinants related to the activity, severity and quality of life of patients with IMIDs as well as to the response and tolerance to treatment.

Enrollment: 2,200 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patient followed for their IMID in one of the departments of the Lille University Hospital participating in the study (dermatology, internal medicine, neurology, pneumology and rheumatology)
• Social insured
• Have the capacity to understand the study requirements, provide written informed consent, and comply with the study data collection procedures.

Exclusion criteria

• Administrative reasons: inability to receive informed information, inability to participate in the entire study, lack of coverage by the social security system.
• Pregnant or breastfeeding woman
• Persons deprived of liberty
• Protected minors or adults
• Persons who have refused or are incapable of giving informed consent
• Persons in Emergency Situations

Trial design

Primary purpose: Other

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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2,200 participants in 1 patient group

IMMINeNT cohort

Experimental group

Treatment:

Other: SF-12 questionnaire

Genetic: Biobanking with genetic analysis