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Clinical Trials in Norway / NCT04009421
Active, not recruiting Observational

Coronary Artery Plaque Burden in Stable Angina and Non-obstructive Coronary Artery Disease

NCT04009421 · tracked via the Priya Life Science Norway tracker
Phase
Observational
Started
2018-02-15
Last updated
2023-11-29

Condition(s) studied

Coronary Artery DiseasePlaque, Atherosclerotic

Investigational drug(s) / intervention(s)

Coronary artery plaque assessment by CT coronary angiography QAngio CT RE

Coronary artery plaque assessment by CT coronary angiography QAngio CT RE: Assessment of segmental plaque volume and composition

Study summary

Non-obstructive coronary artery disease (CAD), particularly common in women, has been associated with impaired quality of life and risk of recurrent hospitalizations. Several studies have also demonstrated increased risk of incident acute coronary events and mortality.

The main objective of the project is to assess the association between coronary artery plaque features by coronary CT angiography and long term prognosis in a large unselected population undergoing CT coronary angiography due to stable angina and suspected myocardial ischemia from the Norwegian Registry for Invasive Cardiology (NORIC) diagnosed with non-obstructive CAD by coronary CT angiography.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Stable angina * Non-obstructive coronary artery disease by CT coronary angiography defined as \<50% stenosis (lumen diameter reduction) Exclusion Criteria: * Obstructive coronary artery disease * Unstable angina * Previous myocardial infarction, heart surgery or percutaneous coronary interventions

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Department of Clinical Science, University of Bergen Bergen Norway

More University of Bergen trials in Norway

Other trials for the same condition

Official registry record

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.

View NCT04009421 on ClinicalTrials.gov ↗ ← All trials in Norway