Proteomics and Genomics Combined With CT to Predict CVD (NCT05800093) | Clinical Trial Compass
Active — Not RecruitingNot Applicable
Proteomics and Genomics Combined With CT to Predict CVD
Netherlands310 participantsStarted 2023-01-12
Plain-language summary
This study evaluates plaque progression and characteristics in patients with coronary atherosclerosis.
Who can participate
Age range50 Years – 75 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Adult patients between 50 and 75 years old
* Subjects at intermediate to high risk for ASCVD
* Asymptomatic patients without cardiac chest pain
* Evidence of atherosclerosis on baseline CCTA
Exclusion Criteria:
* Renal insufficiency, defined as eGFR \< 30 ml/min
* History of cardiovascular events (myocardial infarction, peripheral artery disease and ischemic stroke)
* Use of lipid lowering therapy other than statin, ezetimibe or bempedoic acid monotherapy
* Change in lipid lowering therapy in the last 6 months
* Use of more than two antihypertensive agents
* No coronary atherosclerosis at baseline imaging
* Active malignancy requiring treatment
* Atrial fibrillation
* Any other treatment or clinically relevant condition that could interfere with the conduct or interpretation of the study in the opinion of the investigator
* Inability or unwillingness to comply with the protocol requirements, or deemed by investigator to be unfit for the study.
What they're measuring
1
Coronary Artery Disease Progression
Timeframe: Through study completion, between 130-156 weeks
Trial details
NCT IDNCT05800093
SponsorAcademisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)