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Feasibility of a Cytokine Expression Profile in Immune Cells as an Orientation Tool in Therapeutic Decisions for Auto-inflammatory and Auto-immune Diseases (IL-MAI)

C

Centre Hospitalier Universitaire de Nīmes

Status

Completed

Conditions

Rheumatoid Arthritis

Treatments

Procedure: Blood sample

Study type

Interventional

Funder types

Other

Identifiers

NCT03280797
LOCAL/2016/TAT01

Details and patient eligibility

About

This study will assess the feasibility of using cytokine expression profiles in blood samples as a method for evaluating rheumatoid polyarthritis

Enrollment

44 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • The patient must have given their free and informed consent and signed the consent form
  • The patient must be a member or beneficiary of a health insurance plan
  • Patient is at least 18 years old
  • Subjects included as patients have rheumatoid polyarthritis according to ACR EULA 2010, DAS28>3.2 criteria
  • Subjects included as controls are healthy volunteers who have no overexpression of cytokines

Exclusion criteria

  • The subject is participating in an interventional study, or is in a period of exclusion determined by a previous study
  • The subject refuses to sign the consent
  • It is impossible to give the subject informed information
  • The patient has had at least 3 months of specific treatment that can potentially impact cytokine profile

Trial design

Primary purpose

Screening

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

44 participants in 2 patient groups

Control
Other group
Treatment:
Procedure: Blood sample
Rheumatoid arthritis patients
Other group
Treatment:
Procedure: Blood sample

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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