NCT06713239Active, not recruiting
A Randomized Comparison of Personalized Therapy Mgmt Based On Coronary Atherosclerotic Plaque Vs. Usual Care for Symptomatic Patients With Suspicion of CAD
A Randomized Comparison of Personalized Management for Medical and Interventional Therapy Based On Coronary Atherosclerotic Plaque Versus Usual Care for Symptomatic Patients With Suspicion of CAD
Source: ClinicalTrials.gov · Last updated 5 Jun 2026
Brief summary (registry, in English)
PARAMOUNT is a prospective randomized open-label trial testing the hypothesis that a personalized management strategy in symptomatic patients with suspicion of coronary artery disease (CAD), using a CT-based coronary atherosclerotic plaque assessment by AI-enabled quantitative software improves: certainty for diagnosis of CAD, control of CAD risk factors and efficiency of ICA referral with appropriate PCI compared to the usual care strategy based on current AHA/ACC guidelines for care of symptomatic patients with suspicion of CAD.
- Status (registry)
- Active, not recruiting
- Study type
- Interventional
- Enrollment
- 1000 (estimated)
- First submitted
- 27 Nov 2024
- Start date
- 18 Dec 2024
- Primary completion date
- Dec 2026
- Lead sponsor
- Cleerly, Inc.
- Diseases
- Coronary artery disease
- NCT number
- NCT06713239
What you commit to
- Study type: Interventional
- Planned participants: 1000
- From 18 Dec 2024 to the primary completion date, Dec 2026
- 21 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Currently or previously treated beyond primary prevention guidelines
- Known history of obstructive CAD (prior myocardial infarction, CABG or PCI, stenosis ≥50%)
Other illness
- Suspected acute coronary syndrome or otherwise unstable clinical status
- Planned cardiovascular procedure (e.g. coronary angiography, cardiac surgery, non-coronary vascular procedure)
- Known EF ≤40% or other moderate to severe valvular or congenital cardiac disease
Lab values
- LDL \< 100 mg/dL
- Noninvasive or invasive CV testing for CAD within 1 year (e.g. invasive coronary angiography (ICA), coronary CT angiography (CCTA) including calcium scoring)
Other
- Contraindications to CCTA
Who the study is looking for
- \> 18 years
- Symptomatic patients with suspicion of CAD, including those referred for elective, non-urgent diagnostic testing (e.g. stress test)
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (21)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Capital Cardiology Associates Coordinator of this site? Confirm its status | Albany | United States | Unknown status |
| Flourish Bowie Coordinator of this site? Confirm its status | Bowie | United States | Unknown status |
| St. Louis Heart and Vascular Coordinator of this site? Confirm its status | Bridgeton | United States | Unknown status |
| Intermountain Health Saint Joseph Hospital Coordinator of this site? Confirm its status | Broomfield | United States | Unknown status |
| University of Cincinnatti Coordinator of this site? Confirm its status | Cincinnati | United States | Unknown status |
| Saint Elizabeth Medical Center Coordinator of this site? Confirm its status | Edgewood | United States | Unknown status |
| Endeavor Health Clinical Operations Coordinator of this site? Confirm its status | Evanston | United States | Unknown status |
| Advanced Heart and Vascular Institute of Hunterdon Coordinator of this site? Confirm its status | Flemington | United States | Unknown status |
| Medical City Fort Worth Hospital Coordinator of this site? Confirm its status | Fort Worth | United States | Unknown status |
| Valiance Clinical Research: Huntington Park Coordinator of this site? Confirm its status | Huntington Park | United States | Unknown status |
| The University of Tennessee Medical Center Coordinator of this site? Confirm its status | Knoxville | United States | Unknown status |
| Cardiology Associates of Mobile Coordinator of this site? Confirm its status | Mobile | United States | Unknown status |
| Tulane University Coordinator of this site? Confirm its status | New Orleans | United States | Unknown status |
| Oklahoma Cardiovascular Research Group Coordinator of this site? Confirm its status | Oklahoma City | United States | Unknown status |
| Chippenham and Johnston Willis Hospitals Coordinator of this site? Confirm its status | Richmond | United States | Unknown status |
| Cardiovascular Institute of San Diego Coordinator of this site? Confirm its status | San Diego | United States | Unknown status |
| Tampa Cardiovascular Interventions and Research Coordinator of this site? Confirm its status | Tampa | United States | Unknown status |
| Valiance Clinical Research - Tarzana Coordinator of this site? Confirm its status | Tarzana | United States | Unknown status |
| Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center Coordinator of this site? Confirm its status | Torrance | United States | Unknown status |
| MercyOne Des Moines Medical Center Coordinator of this site? Confirm its status | West Des Moines | United States | Unknown status |
| Flourish Research Coordinator of this site? Confirm its status | Winter Park | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.