Deployment o the Multidisciplinary Prospective Cohort Imminent

RecruitingNot a drug-phase studyMS (type not specified)NCT04334031

What it found

Still running

No result yet.

What was tested

Treatment tested

  • Biobanking with genetic analysis
  • SF-12 questionnaire

What it measured

Main measures

  • Change of SLEDAI for lupus

    once a year for 10 years

    Walking and mobility
  • Change of Medsger score

    once a year for 10 years

  • Change of EDSS for multiple sclerosis

    once a year for 10 years

    Disability progressionFatigue
  • Change of BASDAI for psoriatic arthristis

    once a year for 10 years

    FatiguePain
  • Change of Longhurst criteria for hereditary angioedema

    once a year for 10 years

  • Change of number of flares for atopic dermatitis

    once a year for 10 years

  • Change of number of exacerbations for severe asthma

    once a year for 10 years

  • Change of 12-Item Short-Form Health Survey (SF-12) - quality of life scale

    once a year for 10 years

    Quality of life (reported by participants)
  • number of participant with severe infectious events

    once a year for 10 years

Who could take part

MS (type not specified) · 18 and over

Show the full criteria

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

As registered. Criteria can change, so ask the trial team or your neurologist.

Contact details on the registry

About this trial

In the sponsor's words

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.

Papers

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    History

      1. Started

        Jul 2020

      2. Main results due

        Jul 2031

      3. Finished

        Jul 2031

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