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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02333708
Other study ID # 2013-A00273-44
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date September 2015
Est. completion date November 2023

Study information

Verified date September 2016
Source University Hospital, Caen
Contact Boris BIENVENU, MD, PhD,
Phone +33231064579
Email bienvenu-b@chu-caen.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

To demonstrate that microparticles (MPs), having a powerful procoagulant potential, are in larger amounts in the blood of patients with histologically proven giant cell arteritis (GCA), compared with patients matched for age, sex and with or without inflammatory syndrome.


Recruitment information / eligibility

Status Recruiting
Enrollment 75
Est. completion date November 2023
Est. primary completion date September 16, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility For GCA group: Inclusion Criteria: - Men and women = 18 years of age Patient affiliated to social security regimen - Informed and having signed the consent form to take part in the study. - Diagnosis of GCA, meeting at least 3 of the following 5 American College of Rheumatology (ACR) criteria for the diagnosis of GCA, including inflammatory syndrome and having - Either temporal artery biopsy showing characteristic GCA abnormality - Or inflammatory arteritis on imaging examination Exclusion Criteria: - Persons under protection of the court or guardianship - Inability to understand or to follow study procedures - Dementia - cancer diagnosed within the previous 5 years (except for non-melanoma skin cancer or in situ carcinoma of the cervix)non-contributory or inconclusive temporal artery biopsy - Any conditions that might interfere with MPs level: diabetes, recent endo-arterial gesture, current treatment with corticosteroids. - Participation in another ongoing clinical trial Current anticoagulant therapy - Active infectious disease

Study Design


Intervention

Other:
Blood sample


Locations

Country Name City State
France Centre Hospitalier Universitaire Côte de Nacre Caen

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Caen

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Level of microparticles in the blood of patients with histologically proven giant cell arteritis. Level of microparticles (MPs) in the blood of patients with histologically proven giant cell arteritis (GCA), compared with patients matched for age, sex and with or without inflammatory syndrome. Baseline
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