Using CCTA to Manage Non-Obstructive Coronary Artery Disease
Serial Coronary CTA-based Plaque Progression Detection for Management of Coronary Heart Disease: a Randomised Controlled Trial
NA · Jinling Hospital, China · NCT06843005
This study is testing if using a special heart scan called CCTA to manage non-obstructive coronary artery disease can help people control their cholesterol better and lower their risk of serious heart problems compared to regular care.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 3100 (estimated) |
| Ages | 18 Years to 80 Years |
| Sex | All |
| Sponsor | Jinling Hospital, China (other) |
| Locations | 1 site (Nanjing, Jiangsu) |
| Trial ID | NCT06843005 on ClinicalTrials.gov |
What this trial studies
This study evaluates whether a management strategy based on coronary computed tomography angiography (CCTA) can improve lipid control and reduce major adverse cardiovascular events in patients with non-obstructive coronary artery disease. Participants will be randomly assigned to either a follow-up CCTA management group or a routine clinical management group. The study aims to compare the effectiveness of these two approaches over a three-year period, focusing on the incidence of cardiovascular events and all-cause mortality. The primary goal is to determine if CCTA follow-up leads to better outcomes than traditional management strategies.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18 to 80 with a history of non-obstructive coronary artery disease lasting at least two years.
Not a fit: Patients who have experienced acute coronary syndrome or other significant cardiovascular events may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly reduce the risk of major cardiovascular events in patients with non-obstructive coronary artery disease.
How similar studies have performed: Other studies have shown promise in using imaging techniques for managing coronary artery disease, suggesting this approach may be effective.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Age between 18 and 80 years old; 2. Known patients with non-obstructive coronary artery disease (disease duration ≥2 years); 3. Patients who agree to undergo follow-up CCTA examinations and cooperate in completing follow-up observations. Exclusion Criteria: 1. Patients who have experienced ACS or PCI/CABG; 2. Patients who have experienced adverse cardiovascular and cerebrovascular events; 3. Patients who have undergone follow-up CCTA or DSA examinations before enrollment; 4. Patients with severe hepatic and renal dysfunction; 5. Patients with contraindications to CCTA examinations; 6. Patients with poor initial CCTA image quality or data loss.
Where this trial is running
Nanjing, Jiangsu
- Research Institute Of Medical Imaging Jinling Hospital — Nanjing, Jiangsu, China (RECRUITING)
Study contacts
- Study coordinator: Longjiang Zhang, MD
- Email: kevinzhlj@163.com
- Phone: 13405833167
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Major Adverse Cardiovascular Events, Prevention, Coronary Artery Disease, CT Angiography