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Giant Cell Arteritis - Ways to Precision Medicine

Riesenzellarteriitis - Wege Zur Precision Medicine

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07084480
Enrollment
400
Registered
2025-07-24
Start date
2025-11-14
Completion date
2033-07-31
Last updated
2025-12-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Giant Cell Arteritis, Polymyalgia Rheumatic (PMR)

Keywords

non-interventional cohort study, aortic dilatation, innate lymhoid cells, optic coherence tomography, MRI

Brief summary

Long-term follow-up of aortal adverse events, as well as glucocortioid-associated adverse events in patients with polymyalgia rheumatica (PMR) and giant cell arteritis (GCA).

Detailed description

In this non-interventional cohort study the following aspects should be addressed: * Can regular imaging procedures help to better assess the risk of aortic aneurysms and dissections over a period of 5-10 years after initial diagnosis of GCA? * Which prognostic factors correlate with aortic events? * What conclusions can be drawn about glucocorticoid-associated side effects over the longer (5-year) course? * Can modern imaging in correlation with standardized clinical examination, serological markers and immunophenotypic testing define patient clusters within the clinically heterogeneous disease spectrum of GCA and PMR with the aim of individualizing therapy? * What is the value of orbital MRI together with an ophthalmologic examination including fudoscopy and optical coherence tomography (OCT) in the detection of ischemic manifestations of GCA? * Can a contrast agent-saving MRI technique (with 25 % less contrast agent) be used in GCA without impairing signal quality? * Can rare lymphocyte populations be found by immunophenotyping, which provide information on the probability of recurrence or allow therapy control?

Interventions

None listed

Sponsors

Wuerzburg University Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age greater or similar to 18 years * Primary diagnosis of GCA or PMR

Exclusion criteria

* Age under 18 years * lack of capacity to consent

Design outcomes

Primary

MeasureTime frameDescription
Incidence of aortic adverse eventsWithin 5 yearsAortic adverse events include new foramation or progress of aortic aneurysms, and aortic dissection

Secondary

MeasureTime frameDescription
Incidence of glucocorticoid-related adverse eventswithin 5 yearsAssessment of the glucocorticoid toxicity index (GTI; excluding regular bone density measurements) to detect glucocorticoid-related adverse events. The GIT includes 1) a cumulative worsening score, which includes the cumulative glucocorticoid toxicity over time (minimum value of 0 and a maximum value of 439, a decrease is not possible) and 2) an aggregate improvement score, which allows for decreases and increases of toxicity (range from -346 to 439, with negative values indicating improvement and positive values indicating worsening of glucocorticoid toxicity)
Detection of ischemic complications in the eyeswithin 5 yearsIs orbital MRI together with optic coherence tomography suitable to detect ischemic manifestations of GCA in the eye?
Performance of gadopiclenol in detecting vessel wall inflammationwithin 5 yearsThe contrast agent gadopiclenol should be evaluated for its use in MR angiography, i.e. if it depicts (peri) vessel wall inflammation equally to older contrast agents. In a sub-cohort of 20 % of the patients , MR angiographies will be performed with 25% reduced gadoplicenol.

Countries

Germany

Contacts

Primary ContactMichael Gernert
gernert_m1@ukw.de+4993120140100
Backup ContactHannah Labinsky
Labinsky_h@ukw.de+4993120140100

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026