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RecruitingNCT06843005

Serial Coronary CTA-based Plaque Progression Detection for Management of Coronary Heart Disease

Serial Coronary CTA-based Plaque Progression Detection for Management of Coronary Heart Disease: a Randomised Controlled Trial

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
3,100 (estimated)
Sponsor
Zhang longjiang,MD · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

The primary objective of this study is to evaluate whether a management strategy based on coronary computed tomography angiography (CCTA) for patients with non-obstructive coronary artery disease can improve the LDL-C target achievement rate compared to a traditional management strategy without follow-up CCTA, thereby reducing the incidence of major adverse cardiovascular and cerebrovascular events over a 3 years period, including all-cause mortality, myocardial infarction, ischemia driven revascularation and stroke.

Detailed description

Patients with non-obstructive coronary artery disease have a high rate of adverse cardiovascular events, and currently, there is still a lack of effective management strategies for these patients in clinical practice. In the SUCCESS study, investigator will compare follow-up CCTA management with routine clinical management to assess the effectiveness of follow-up CCTA in improving lipid control and reducing cardiovascular events in these patients. The SUCCESS study is a multicenter, randomized, parallel-controlled, interventional clinical trial that recruits patients with non-obstructive coronary artery disease identified on previous CCTA (coronary artery stenosis of 20% to 70% or left main coronary artery stenosis of 20% to 50%). The experimental group is the CCTA follow-up management group, and the control group is the routine clinical follow-up management group. All participants will be randomly assigned to the experimental and control groups in a 1:1 ratio. The experimental group will undergo management using follow-up CCTA, while the control group will be managed using routine clinical and laboratory examinations. At the 1-year follow-up, all participants will undergo laboratory re-examination to observe the impact of follow-up CCTA on lipid target achievement. After 3 years of follow-up, the differences in the occurrence of major adverse cardiovascular and cerebrovascular events (MACCE) between the two groups will be compared.

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TESTCoronary Computed Tomography AngiographyBased on the assessment of plaque progression after follow-up CCTA examination, patients will be given either intensive treatment or routine treatment.
OTHERCurrent clinical guidelinesPatients will be treated according to the 2024 ESC Guidelines for the Management of Chronic Coronary Syndromes.

Timeline

Start date
2025-02-28
Primary completion
2028-12-30
Completion
2028-12-30
First posted
2025-02-24
Last updated
2026-03-24

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT06843005. Inclusion in this directory is not an endorsement.