Coronary Heart Disease Clinical Trials

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Prospective RandomizEd Evaluation and Management of Premature aTherosclerosis

Status: Recruiting
Location: See all (23) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 3
SUMMARY

Heart disease is the leading cause of death for men, women, and people of most racial and ethnic groups in the United States. This clinical trial will test if screening and early treatment of mild heart disease works. PRE-EMPT will screen individuals at low 10-year risk of heart disease with heart disease risk factors to identify those who already have early cholesterol build up, also called plaque, in their heart arteries. It consists of two phases: 1. A Screening Study - Participants will be assessed for plaque by one or both of these scans. * Coronary Artery Calcium (CAC) Scan: A CT scan that looks for calcium or plaque in heart arteries. * Coronary CT Angiography (CCTA) Scan: A CT scan that uses contrast dye to create detailed 3D pictures of heart arteries to look for plaque. 2. A Treatment Trial (approximately 1,500 participants) - Based on the results of the CCTA, participants may be randomized into a two-year trial to test medications aimed at reducing or stabilizing plaque. Participants will have a 1 in 4 chance of receiving only placebo, and a 3 in 4 chance of receiving at least one active medication. Participants will take two pills once a day-either both active medications, one active and one placebo, or both placebos. * Rosuvastatin 20 mg: a cholesterol-lowering medicine * Colchicine 0.5 mg: a medication that lowers inflammation Everyone in the trial will be given information and advice on heart-healthy diet and lifestyle. Participants will have up to two in-person visits for the screening study, then phone visits for the Treatment Trial at the beginning, 3 months, 12 months and 24 months when they will also have an in-person visit for a CCTA Scan. Participants will have blood drawn using an at-home collection device mailed to their home at the beginning, 3 months, and end of the study.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 30
Maximum Age: 60
Healthy Volunteers: f
View:

• Women aged 40-60 years; Men aged 30-50 years

• Willing and able to provide informed consent and comply with study procedures

• Smart phone user

• Use of highly effective contraception by females with reproductive potential.

• CAC score 1-99 in the screening study or entry through the known plaque pathway (with mild CAC or CAC\<100 if known; elevated CAC on baseline CCTA is not exclusionary in the known plaque arm)

• Diagnostic baseline CCTA with NCPV ≥10 mm3 as assessed by the central core lab

Locations
United States
Alabama
University of Alabama at Birmingham
RECRUITING
Birmingham
Cardiology Associates
RECRUITING
Mobile
California
Lundquist Institute for Biomedical Innovation at Harbor UCLA Medical Center
RECRUITING
Los Angeles
University of California, Los Angeles
RECRUITING
Los Angeles
Georgia
Wellstar Kennestone Hospital
RECRUITING
Hiram
Illinois
University of Chicago
NOT_YET_RECRUITING
Chicago
Massachusetts
Massachusetts General Hospital Brigham
NOT_YET_RECRUITING
Boston
Maryland
Johns Hopkins University
NOT_YET_RECRUITING
Baltimore
Minnesota
Essentia Health
NOT_YET_RECRUITING
Duluth
North Carolina
Duke University Hospital
RECRUITING
Durham
Wake Forest University, Advocate Health
NOT_YET_RECRUITING
Winston-salem
New York
Northern Westchester Hospital
NOT_YET_RECRUITING
Mount Kisco
New York University Langone
NOT_YET_RECRUITING
New York
Weill Cornell Medicine
RECRUITING
New York
Oregon
Oregon Health and Sciences University
NOT_YET_RECRUITING
Portland
Pennsylvania
Thomas Jefferson University
NOT_YET_RECRUITING
Philadelphia
University of Pittsburgh Medical Center
NOT_YET_RECRUITING
Pittsburgh
South Carolina
Medical University of South Carolina (MUSC)
NOT_YET_RECRUITING
Charleston
Tennessee
Vanderbilt University
NOT_YET_RECRUITING
Nashville
Texas
Houston Methodist Hospital
NOT_YET_RECRUITING
Houston
Virginia
University of Virginia (UVA)
NOT_YET_RECRUITING
Charlottesville
Inova Health System
NOT_YET_RECRUITING
Fairfax
Wisconsin
Marshfield Clinical Research Institute
NOT_YET_RECRUITING
Marshfield
Contact Information
Primary
Rachel Olson, Project Manager
rachel.e.olson@duke.edu
919-309-5544
Time Frame
Start Date: 2026-07-21
Estimated Completion Date: 2031-07
Participants
Target number of participants: 1500
Treatments
Experimental: rosuvastatin 20mg plus colchicine-matched placebo
statin plus placebo (two pills once daily)
Experimental: colchicine 0.5mg plus rosuvastatin-matched placebo
anti-inflammatory plus placebo (two pills once daily)
Experimental: rosuvastatin 20mg plus colchicine 0.5mg
statin plus anti-inflammatory (two pills once daily)
Placebo_comparator: placebo plus placebo
Placebo and placebo (two pills once daily)
Related Therapeutic Areas
Sponsors
Leads: Duke University
Collaborators: Massachusetts General Hospital, Johns Hopkins University, National Heart, Lung, and Blood Institute (NHLBI), University of North Carolina, Chapel Hill

This content was sourced from clinicaltrials.gov