Giant Cell Arteritis (GCA) Clinical Trials

Find Giant Cell Arteritis (GCA) Clinical Trials Near You

Disease Activity Monitoring in Patients With Giant Cell Arteritis

Status: Recruiting
Location: See all (7) locations...
Study Type: Observational
SUMMARY

Giant Cell Arteritis (GCA) is a vasculitis of medium- and large-sized arteries in older adults that may lead to serious vascular complications, including permanent vision loss and aortic aneurysm formation. Glucocorticoids are effective, but relapse during tapering is common and poses a major clinical challenge, potentially contributing to prolonged glucocorticoid exposure. Symptoms are often nonspecific and conventional inflammatory markers lack sufficient reliability, particularly in patients treated with drugs targeting the interleukin-6 pathway. Thus, this project aims to evaluate different tools assisting disease activity monitoring and/or predict future relapses and higher treatment requirements. Up to 175 patients with GCA in remission will be enrolled to ensure that 144 participants complete 1 year of follow-up. Participants undergo vascular ultrasonography, including double-blinded assessment at suspected relapse, complete patient-reported outcome measures, and provide biobank blood samples.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 50
Healthy Volunteers: f
View:

• Clinical GCA diagnosis established/confirmed by a rheumatologist and positive GCA imaging or biopsy at diagnosis \< 3 years.

• Clinical remission at the time of inclusion, defined as

‣ Having adhered for ≥ 8 weeks prior to inclusion to either (a) the planned tapering of glucocorticoid therapy, or (b) the planned glucocorticoid-sparing DMARD treatment (with or without glucocorticoids).

⁃ Absence of, or no worsening of, symptoms attributed to GCA in ≥ 8 weeks.

⁃ Normal CRP level (\< 10 mg/L) within 7 days before inclusion.

• Current prednisolone dosage of ≥ 5 mg if glucocorticoid monotherapy.

• A continuous tapering of monotherapy or combination therapy is planned.

• Age \> 50 years.

• Study participants must be able to speak and understand spoken and written Danish.

Locations
Other Locations
Denmark
Aalborg University Hospital, Department of Rheumatology
NOT_YET_RECRUITING
Aalborg
Aarhus University Hospital, Department of Rheumatology
NOT_YET_RECRUITING
Aarhus
Rigshospitalet Glostrup, Center for Rheumatology and Spine Diseases Rigshospitalet
NOT_YET_RECRUITING
Glostrup Municipality
Regional Hospital Horsens, Department of Medicine
RECRUITING
Horsens
Hospitalsenhed Midt, Medicinsk Diagnostisk Center
NOT_YET_RECRUITING
Silkeborg
Svendborg Hospital, Department of Medicine
NOT_YET_RECRUITING
Svendborg
Vejle Hospital, Department of Medicine
NOT_YET_RECRUITING
Vejle
Contact Information
Primary
Morten Hansen, Medical Doctor
mothas@rm.dk
+45 20187463
Time Frame
Start Date: 2026-05-06
Estimated Completion Date: 2029-02
Participants
Target number of participants: 175
Sponsors
Collaborators: Svendborg Hospital, Regionshospitalet Silkeborg, Horsens Hospital, Aalborg University Hospital, Vejle Hospital, Glostrup University Hospital, Copenhagen, Aarhus University Hospital
Leads: University of Aarhus

This content was sourced from clinicaltrials.gov