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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

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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.

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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

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Data and sources

Registry record
Listed on ClinicalTrials.gov.
Official title
The VGR GCA Cohort
Record updated
15 April 2026