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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT04789278
Other study ID # ICC-QI-2021
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date March 30, 2021
Est. completion date September 15, 2022

Study information

Verified date July 2022
Source Stanford University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This is a multi-center, randomized quality improvement project. At least 200 statin-naïve patients without a history of atherosclerotic cardiovascular disease with incidental coronary artery calcium (CAC) on a prior non-gated chest CT will be enrolled across the Stanford Healthcare System and the Palo Alto Veteran's Affairs Healthcare System. Patients will be randomized in a 1:1 fashion to notification or usual care arms. The primary aim of this project is to estimate the increase in 6-month statin prescription among statin-naïve patients without a history of atherosclerotic cardiovascular disease with incidental CAC on a non-gated chest CT who are randomized to receive notification of their findings vs. usual care.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 173
Est. completion date September 15, 2022
Est. primary completion date January 15, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria: - Non-gated chest CT between 2014-2019 - The presence of CAC confirmed by manual review by an experienced radiologist - Stanford affiliated primary care provider or endocrinologist for Stanford healthcare system patients and VA primary care provider for VA patients with at least 1 encounter since 2018 Exclusion Criteria: - Current or prior statin or PCSK9 inhibitor therapy - Prior diagnosis of ASCVD (coronary artery disease, peripheral arterial disease, cerebrovascular disease, coronary/peripheral revascularization) - Prior coronary imaging (cardiac CT, invasive coronary angiography) - Dementia - Metastatic cancer or active cancer undergoing chemotherapy - History of medical nonadherence

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Notification
Notification of coronary calcium to the patient and their clinician

Locations

Country Name City State
United States Stanford Hospital & Clinics Stanford California

Sponsors (1)

Lead Sponsor Collaborator
Stanford University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Rate of Statin Prescription Proportion of patients prescribed a statin Within 6 months
Secondary Statin Intensity Proportion of patients prescribed a high intensity, intermediate intensity, and low intensity statin 6 months
Secondary Total Cholesterol Level 6 months
Secondary LDL Cholesterol Level 6 months
Secondary HDL Cholesterol Level 6 months
Secondary Triglyceride Level 6 months
Secondary Systolic Blood Pressure 6 months
Secondary Number of Hypertension Medications 6 months
Secondary Hemoglobin A1c Level 6 months
Secondary Body Mass Index 6 months
Secondary Pooled cohort equations estimated 10-year risk of atherosclerotic cardiovascular disease 6 months
Secondary Rate of Aspirin Prescription Proportion of patients prescribed aspirin 6 months
Secondary Number of primary Care Clinical Encounters 6 months
Secondary Number of Cardiology Referrals 6 months
Secondary Number of Cardiovascular Diagnostic Tests 6 months
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