New MRI method could replace scalpel for diagnosing head artery disease
NCT ID NCT05865054
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This study is testing whether a special MRI scan can detect inflammation in the arteries that supply blood to the head, brain, and eyes in people with suspected giant cell arteritis (GCA). Researchers will enroll 400 adults aged 50 and older who have new or worsening symptoms and plan to undergo a biopsy or ultrasound for diagnosis. The goal is to see if MRI can accurately identify artery inflammation, potentially offering a less invasive way to diagnose this condition.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Magnetic Resonance Imaging (MRI) with contrast
- What this could lead to
- If successful, MRI could become a reliable, non-invasive way to diagnose giant cell arteritis, reducing the need for surgical biopsies.
- What could go wrong
- This is an observational study, not a treatment trial. MRI may not be accurate enough to replace current diagnostic methods, and results may vary across patients.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 400 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jul 2020
- Expected to finish
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Jul 2033
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Participants will be recruited from the ambulatory clinic, emergency department, or inpatient settings.
- Ages
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50 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age 50 years or older * First presentation of suspected GCA * New or worsening cranial manifestations within 4 weeks of enrollment concerning for active GCA * Elevated CRP greater than 1.0 mg/dl * Plan to undergo temporal artery biopsy or ultrasound for diagnosis Exclusion Criteria: * Contra-indication to receiving MRI including: Implanted medical devices, pacemaker, and metallic foreign fragments inside body/orbits Known gadolinium allergy Women who are pregnant or nursing * Absence of cranial symptoms related to GCA (e.g., only large vessel GCA)
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
4 sites in 3 countries. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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3400 Civic Center Blvd
RECRUITINGPhiladelphia, Pennsylvania, 19104, United States
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Mayo Building and Gonda Building
RECRUITINGRochester, Minnesota, 55905, United States
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St. Joseph's Healthcare Hamilton
NOT_YET_RECRUITINGHamilton, Ontario, L8G 5E4, Canada
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University Hospital Wuerzburg
NOT_YET_RECRUITINGWürzburg, Würzburg, 97080, Germany
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