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Completed

NCT Number: NCT05248906

Giant Cell Arteritis - Optimization of Diagnostics

Giant cell arteritis - Optimization of diagnostics

Completed

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Key information

About this study

A prospective study. Investigating the use of ultrasound, temporal artery biopsy, biomarkers and 18F-fluorodeoxyglucose positron emission tomography-computed tomography for establishing a diagnosis of giant cell (temporal) arteritis.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Clinical suspicion of giant cell arteritis

Meets the American College of Rheumatology Criteria:

Age at disease onset => 50 years New headache Temporal artery abnormality Elevated erythrocyte sedimentation rate >=50 mm/hour Abnomal artery biopsy

Exclusion criteria

Active cancer Use of steroid for more than a week (the prior 6 months)

Treatment and study plan

Giant cell arteritis

Diagnostic Test

Ultrasound 18F-fluorodeoxyglucose (18F-FDG) Positron Emission Tomography Temporal artery biopsy

Primary outcomes

  1. Giant cell arteritis

    Time frame: Week 26

    Clinical verification of giant cell arteritis diagnosis as evaluated with a combination of ultrasound, biopsy and PET/CT.

Sponsors and collaborators

Lead sponsor

Rigshospitalet, Denmark

Other

Registry information

Official study title

Giant Cell Arteritis - Examination of the Optimal Diagnostic Pathway

Acronym: GAME

Important dates

Study start
2021
Primary completion
2024
Study completion
2024
First posted
Feb 21, 2022
Registry last updated
Apr 2, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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