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Collection and Analysis of the Clinical and Biological Characteristics of Patients Treated for Giant Cells ARTEitis (Horton's Disease) (CARTECEL)

C

Centre Hospitalier Universitaire de Nīmes

Status

Completed

Conditions

Giant Cell Arteritis
Horton Disease

Treatments

Other: no intervention

Study type

Observational

Funder types

Other

Identifiers

NCT04142515
Local2019/RG-01

Details and patient eligibility

About

Giant cell arteritis (GCA) or Horton's disease: frequent large vessel vasculitis (cephalic) (incidence estimated at 9 per 100,000 in France), potentially responsible for blindness.

Treatment: corticosteroid therapy, which is effective in the vast majority of cases.

Clinical problem: relapse; 36% to 44% of patients have a relapse that occurs in the first year for many patients, requiring a re-escalation of corticosteroid therapy, with its consequences:

  • Cumulative dose of corticosteroid therapy that causes cardiovascular and infectious morbidity.
  • Requires additional immunosuppressive treatment.

Enrollment

83 patients

Sex

All

Ages

45+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients aged 45 years or older
  • Patients with giant cell arteritis according to ACR criteria or revised criteria incorporating imaging parameters,
  • Patients managed at the University Hospital of Carémeau in Internal Medicine from 01/01/2011 to 01/01/2020.

Exclusion criteria

None

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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