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Proteomics and Genomics Combined With CT to Predict CVD (PREDICT-CVD)

A

Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

Status

Active, not recruiting

Conditions

Coronary Artery Disease Progression

Study type

Observational

Funder types

Other

Identifiers

NCT05800093
NL81913.018.22

Details and patient eligibility

About

This study evaluates plaque progression and characteristics in patients with coronary atherosclerosis.

Enrollment

310 patients

Sex

All

Ages

50 to 75 years old

Volunteers

No Healthy Volunteers

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.

Trial contacts and locations

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Central trial contact

Erik SG Stroes, MD PhD

Data sourced from clinicaltrials.gov

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