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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02343770
Other study ID # 9355
Secondary ID
Status Recruiting
Phase N/A
First received January 7, 2015
Last updated September 4, 2015
Start date June 2015
Est. completion date December 2016

Study information

Verified date September 2015
Source University Hospital, Montpellier
Contact n/a
Is FDA regulated No
Health authority France: Agence Nationale de Sécurité du Médicament et des produits de sant
Study type Interventional

Clinical Trial Summary

Juvenile idiopathic arthritis (JIA) is the most common form of arthritis in children. The etiology is unknown. Several types of arthritis fall under the JIA heading. Oligoarticular JIA with antinuclear antibodies affects about half of all children. There 's no specific markers. Our purpose is to identify new markers in this pathology. The ProtoArray®Human Protein Microarray allows rapid and efficient detection of protein interaction using a suitable protein or small molecule probe. The investigators hope so detect novel potential autoantigen biomarkers specific in JIA.


Description:

We select 10 patients with inclusion criteria and 10 controls. We analyse their blood sample (5ml). The ProtoArray® Microarray allows to detect novel protein-protein interactions, to rapidly perform serum profiling using a sensitive method to detect potential autoantigen biomarkers. The ProtoArray® Human Protein Microarray is a high-density protein microarray containing thousands of purified human proteins for protein interaction screening.


Recruitment information / eligibility

Status Recruiting
Enrollment 20
Est. completion date December 2016
Est. primary completion date December 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 2 Years to 16 Years
Eligibility Inclusion Criteria for experimental group :

- child age from 2 to 16 years

- Oligoarticular JIA with antinuclear antibodies

- with or without uveitis

Exclusion criteria for experimental group :

- immunosuppressive and biological therapy

Inclusion Criteria for control group :

- child age from 2 to 16 years

Study Design

Allocation: Non-Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Diagnostic


Intervention

Other:
blood sample for identifying biomarkers


Locations

Country Name City State
France Cardiology paediatric consultation, Arnaud de Villeneuve Hospital Montpellier

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Montpellier

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary identification of specific autoantigen biomarkers Identify blood sampling biomarkers of juvenile idiopathic arthritis 1 day No
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