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NCT04794868: DESTINY
PreDiction and Validation of Clinical CoursE of Coronary Artery DiSease With CT-Derived Non-Invasive HemodYnamic Phenotyping and Plaque Characterization (DESTINY Study)
trial testing CCTA-derived high risk plaque characteristics in Acute Coronary Syndrome in 356 participants. Completed in 31 December 2024.
31 December 2024
Quick facts
| Lead sponsor | Samsung Medical Center |
|---|---|
| Status | Completed |
| Study type | OBSERVATIONAL |
| Enrollment | 356 |
| Start date | 1 April 2020 |
| Primary completion | 31 December 2024 |
| Estimated completion | 31 December 2024 |
| Sites | 2 locations across China, South Korea |
Drugs / interventions tested
- CCTA-derived high risk plaque characteristics
- CFD-derived hemodynamic parameters
Conditions studied
- Acute Coronary Syndrome — all drugs for Acute Coronary Syndrome →
- Ischemic Heart Disease — all drugs for Ischemic Heart Disease →
Sponsor
Samsung Medical Center
Who can join
Eligibility, any sex, with Acute Coronary Syndrome or Ischemic Heart Disease. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Acute coronary syndrome (ACS) and sudden cardiac death can be the first manifestation of coronary artery disease and are the leading cause of death in the majority of the world's population. The main pathophysiology of ACS is well-known and fibrous cap thickness, presence of a lipid core, and the degree of inflammation have been proposed as the key determinants of plaque vulnerability. Previous studies using virtual histology intravascular ultrasound or optical coherence tomography showed that clinical application of this concept improved risk prediction of ACS. However, these approaches have not been widely adopted in daily practice due to relatively low positive predictive values, low prevalence of high-risk plaques and the invasive nature of diagnostic modalities. Non-invasive imaging studies with coronary computed tomography angiography (CCTA) also showed the clinical value of CCTA-derived high risk plaque characteristics (HRPC). In addition, the recent progress in CCTA and computational fluid dynamics (CFD) technologies enables simultaneous assessment of anatomical lesion severity, presence of HRPC and quantification of hemodynamic forces acting on plaques in patient-specific geometric models. As plaque rupture is a complicated biomechanical process influenced by the structure and constituents of the plaque as well as the external mechanical and hemodynamic forces acting on the plaque, a comprehensive evaluation of lesion geometry, plaque characteristics and hemodynamic parameters may enhance the identification of high-risk plaque and the prediction of ACS risk. In this regard, the current study is designed to evaluate prognostic implications of comprehensive non-invasive hemodynamic assessment using CCTA and CFD in the identification of high risk plaques that caused subsequent ACS.
Publications & conference data
3 peer-reviewed publications reference this trial (live from Europe PMC):
-
Anatomic and Hemodynamic Plaque Characteristics for Subsequent Coronary Events.
Lee SH, Hong D, Dai N, Shin D, et al · · 2022 · cited 13× · PMID 35677691 · DOI 10.3389/fcvm.2022.871450 -
Fractional Flow Reserve and Fractional Flow Reserve Gradient From CCTA for Predicting Future Coronary Events.
Hong D, Dai N, Lee SH, Shin D, et al · · 2024 · cited 1× · PMID 39553907 · DOI 10.1016/j.jacasi.2024.06.007 -
Biomechanical index for predicting the risk of acute coronary syndrome.
Johnson MJ, Abdelmalik MRA, Choi G, Hossain SS, et al · · 2026 · PMID 41953669 · DOI 10.3389/fcvm.2026.1766059
Verify or expand the search:
- PubMed search for NCT04794868
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT04794868 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Samsung Medical Center
- Last refreshed: 14 March 2025
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Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing