DECT;CCTA: Perform DECT and CCTA examinations on the patient
Study summary
This observational study aims to evaluate the association between sodium urate deposition volume and coronary atherosclerotic plaques in patients with foot gout using dual-energy CT (DECT) and coronary CTA. This study will explore imaging-based evidence for the progression and risk prediction of adverse cardiovascular events in patients with gout.
Eligibility
Sex
ALL
Min age
18 Years
Max age
90 Years
Healthy volunteers
No
Inclusion Criteria:
* Aged ≥18 years, male or female
* Clinically diagnosed with podagra
* Having high-risk factors for cardiovascular disease
* Complete clinical data available
* Patients and their family members are informed, consent and have signed the informed consent form
Exclusion Criteria:
* Women who are preparing for pregnancy, pregnant or breastfeeding
* Male and female subjects of reproductive age who are unable to take effective contraceptive measures
* Patients who cannot or are unable to undergo CTA scans
* Patients with severe heart diseases such as severe heart failure, severe heart valve disease and cardiomyopathy
* Severe hemodynamic instability
* Any other reason making subjects unsuitable to participate in the study, including subjects who are unable or unwilling to comply with the requirements of the study protocol
Primary outcome measure(s)
Volume of sodium urate deposition and coronary artery plaque volume — baseline Measurement of sodium urate deposition volume and coronary artery plaque volume in patients with foot gout.
Trial sites (1)
Facility
City
Region
Status
The Affiliated Hospital of Qingdao University
Qingdao
Shandong
More The Affiliated Hospital of Qingdao University trials in China
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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