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

NCT ID: NCT03280797

Last Updated: 2022-01-25

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

44 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-11-24

Study Completion Date

2022-01-12

Brief Summary

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

Detailed Description

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Conditions

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Rheumatoid Arthritis

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

SCREENING

Blinding Strategy

NONE

Study Groups

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Control

Group Type OTHER

Blood sample

Intervention Type PROCEDURE

2ml blood taken into TruCulture tube

Rheumatoid arthritis patients

Group Type OTHER

Blood sample

Intervention Type PROCEDURE

2ml blood taken into TruCulture tube

Interventions

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Blood sample

2ml blood taken into TruCulture tube

Intervention Type PROCEDURE

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Centre Hospitalier Universitaire de Nīmes

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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CHU de Montpellier

Montpellier, , France

Site Status

CHU Nimes

Nîmes, , France

Site Status

Countries

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France

Other Identifiers

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LOCAL/2016/TAT01

Identifier Type: -

Identifier Source: org_study_id

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