The Correlation Between Sodium Urate (MSU) Deposition and Coronary Atherosclerosis in Patients With Foot Gout
Affiliated Hospital of Qingdao University
1 other identifier
observational
200
1 country
1
Brief 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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Aug 2026
Typical duration for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
August 18, 2026
CompletedStudy Start
First participant enrolled
August 20, 2026
CompletedFirst Posted
Study publicly available on registry
August 25, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2028
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 1, 2028
August 25, 2026
August 1, 2026
2.3 years
August 18, 2026
August 20, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
Volume of sodium urate deposition and coronary artery plaque volume
Measurement of sodium urate deposition volume and coronary artery plaque volume in patients with foot gout.
baseline
Interventions
Perform DECT and CCTA examinations on the patient
Eligibility Criteria
Patients with podagra who have high-risk factors for cardiovascular disease
You may qualify if:
- 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
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
The Affiliated Hospital of Qingdao University
Qingdao, Shandong, 266003, China
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
August 18, 2026
First Posted
August 25, 2026
Study Start
August 20, 2026
Primary Completion (Estimated)
December 1, 2028
Study Completion (Estimated)
December 1, 2028
Last Updated
August 25, 2026
Record last verified: 2026-08
Data Sharing
- IPD Sharing
- Will not share