The VGR GCA Cohort: Ultrasound, Biopsy and Biomarkers - Novel Methods for Diagnosis, Monitoring and Prognosis in Giant Cell Arteritis.
Key facts
- Who runs it
- Vastra Gotaland Region
- Where
- Sweden1 site in 1 countryChoose a country to see its sites
- Trial code
- Status
- Recruiting
- People taking part
- 340 people, planned
- Started
- 1 Mar 2026
- Expected to end
- 1 Dec 2029
- Type of study
- Observational, 2 groups
- Record updated
- 15 April 2026
Who can take part
- Age
- 18 years and older
- Sex
- Women and men
- Healthy volunteers
- Can take part
The registry criteria, word for word
Show all 7 criteriaShow less
Who can take part
- Individuals referred for evaluation due to suspected giant cell arteritis (GCA)
- Ability to provide written informed consent
Who cannot take part
- Previous diagnosis of GCA
- Previous temporal artery biopsy performed as part of prior GCA evaluation
- Treatment with high-dose corticosteroids (>7.5 mg/day) for more than two weeks before initiation of the diagnostic work-up
- Inability to provide informed consent
- Inability to comply with the study protocol
This trial has no sites in United States.
It has sites in one country. Choose a country to see its sites.
About the trial
What the trial wants to find out
Giant cell arteritis (GCA) is the most common vasculitis in the elderly and is usually treated with long-term corticosteroid therapy. Many patients experience relapses and treatment-related side effects. Current diagnostic and monitoring methods provide limited prognostic information and cannot reliably distinguish active from inactive disease during relapse. This project addresses the clinical need for improved tools to identify patients at high risk of relapse and to develop more effective methods for disease monitoring.
Read full original descriptionShow less
The aim is to develop new tools that enable more personalized treatment of GCA. By combining vascular ultrasound with novel blood biomarkers, we seek to predict disease course and relapse risk. The specific objectives are:
* To identify ultrasound and blood biomarkers that can predict long-term disease control. * To determine which ultrasound parameters and blood biomarkers can distinguish active from inactive disease during treatment. * To evaluate whether extended vascular ultrasound protocols can improve diagnostic accuracy.
The ultimate goal is to establish safe, practical tools for improved diagnosis and follow-up in patients with GCA.
The 2 groups in the trial
- GCA group
Individuals diagnosed with GCA
- Control group
Individuals not diagnosed with GCA
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Contact the study team: see the registry record → Contacts and Locations
Print a page for my doctorData and sources
- Registry record
- Listed on ClinicalTrials.gov.
- Official title
- The VGR GCA Cohort
- Record updated
- 15 April 2026