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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05977413
Other study ID # 71202
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date July 2024
Est. completion date June 2030

Study information

Verified date July 2023
Source Stanford University
Contact David J Maron, MD
Phone 650-724-6152
Email david.maron@stanford.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This trial will investigate whether notifying patients and their clinicians of the presence of moderate or severe coronary artery calcium on a low-dose CT scan performed for lung cancer screening results in a lower incidence of cardiovascular death, nonfatal myocardial infarction, or nonfatal stroke as compared with usual care informed by clinical practice guidelines.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 40000
Est. completion date June 2030
Est. primary completion date June 2030
Accepts healthy volunteers No
Gender All
Age group 50 Years to 84 Years
Eligibility Inclusion Criteria: - Age 50-84 years - No known ASCVD - Lung cancer screenee with low dose CT scan (LDCT) within the last 5 years - Coronary artery calcium (CAC) score on LDCT >100 Agatston units (AU) - Not taking a statin or other lipid-lowering therapy (e.g., ezetimibe, bempedoic acid, or PCSK9-lowering therapy) Exclusion Criteria: - Dementia or other neuropsychiatric disorder that interferes with medication adherence - CAC scan, coronary CT angiogram, or invasive angiogram since LDCT - Statin medication intolerance or allergy - Life expectancy <2 years, e.g., metastatic cancer or active cancer undergoing chemotherapy

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Notification of CAC
Provider and patient are notified of coronary artery calcium present on patient's CT scan. Notification includes a personalized image of CAC from the patient's CT scan performed for lung cancer screening.
Usual Care
Patients randomized to Usual Care will receive usual medical care provided by their clinician informed by widely publicized clinical practice guidelines.

Locations

Country Name City State
n/a

Sponsors (3)

Lead Sponsor Collaborator
Stanford University Duke University, Patient-Centered Outcomes Research Institute

References & Publications (2)

Eng D, Chute C, Khandwala N, Rajpurkar P, Long J, Shleifer S, Khalaf MH, Sandhu AT, Rodriguez F, Maron DJ, Seyyedi S, Marin D, Golub I, Budoff M, Kitamura F, Takahashi MS, Filice RW, Shah R, Mongan J, Kallianos K, Langlotz CP, Lungren MP, Ng AY, Patel BN. Automated coronary calcium scoring using deep learning with multicenter external validation. NPJ Digit Med. 2021 Jun 1;4(1):88. doi: 10.1038/s41746-021-00460-1. — View Citation

Sandhu AT, Rodriguez F, Ngo S, Patel BN, Mastrodicasa D, Eng D, Khandwala N, Balla S, Sousa D, Maron DJ. Incidental Coronary Artery Calcium: Opportunistic Screening of Previous Nongated Chest Computed Tomography Scans to Improve Statin Rates (NOTIFY-1 Project). Circulation. 2023 Feb 28;147(9):703-714. doi: 10.1161/CIRCULATIONAHA.122.062746. Epub 2022 Nov 7. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Other Rate of Specific Statin Prescribed and Statin Dose Rate of prescription of specific statins at specific doses 1 year post randomization
Other Rate of Prescription of Non-statin Lipid-lowering Medications Rate of prescription of specific non-statins 1 year post randomization
Other Rate of Aspirin Prescription Rate of aspirin prescription by treatment group 1 year post randomization
Other Number of Antihypertensive Medications Number of antihypertensive medications prescribed per participant by treatment group 1 year post randomization
Other Median LDL-C Concentration Median LDL cholesterol concentration by treatment group 1 year post randomization
Other Percentage of participants with LDL-C <70 mg/dL Percentage of participants with LDL-C <70 mg/dL by treatment group 1 year post randomization
Other Systolic blood pressure Median systolic blood pressure value in mmHg by treatment group 1 year post randomization
Other Percentage of participants with Systolic Blood Pressure <130 mmHg Percentage of participants with systolic blood pressure <130 mmHg by treatment group 1 year post randomization
Other Body Mass Index Median body mass index value by treatment group 1 year post randomization
Other Total number of primary care clinical encounters during the trial 6 years
Other Number of cardiology encounters 6 years
Other Number of cardiovascular diagnostic noninvasive tests 6 years
Primary Time to first occurrence of cardiovascular death, nonfatal myocardial infarction, or nonfatal stroke 6 years
Secondary Rate of All-cause Death Number (%) of participants in each treatment group with death from any cause. 6 years
Secondary Rate of Cardiovascular Death Number (%) of participants in each treatment group with cardiovascular death 6 years
Secondary Rate of Nonfatal Myocardial Infarction Number (%) of participants in each treatment group with nonfatal myocardial infarction 6 years
Secondary Rate of Nonfatal Stroke Number (%) of participants in each treatment group with nonfatal stroke 6 years
Secondary Initial lipid-lowering therapy prescription rate Number (%) of participants in each treatment group with active prescriptions of lipid-lowering therapy at 6 months following randomization within 6 months of 1st notification
Secondary Number of Participants with active lipid-lowering therapy prescriptions Persistence of need for lipid-lowering therapy at 18 months following randomization. At 18 months
Secondary Number of revascularization procedures (PCI, CABG, carotid artery revascularization, or peripheral artery revascularization) Number of revascularization procedures (PCI, CABG, carotid artery revascularization, or peripheral artery revascularization) 6 years
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