Actively Recruiting
Early Screening and Risk Assessment of Polyvascular Disease Using Multi-Modality Imaging and Artificial Intelligence A Study Sponsored by Harbin Medical University
Led by Harbin Medical University · Updated on 2024-12-27
1100
Participants Needed
1
Research Sites
115 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are investigating polyvascular disease (PVD) using advanced imaging and artificial intelligence to improve early detection and treatment. The study aims to create a comprehensive imaging database for PVD, develop a one-stop screening process, and establish a multidisciplinary approach for diagnosis and treatment. It also seeks to build a combined "eye-heart-brain" warning model using non-invasive imaging techniques and explore molecular communication pathways to identify potential targets for intervention and risk assessment. Participants will undergo multiple imaging tests including Magnetic Resonance Angiography of various arteries and CT angiography of coronary or intracranial arteries. The study combines ocular OCTA with CTA imaging to develop an integrated early warning system. The research also involves collecting multi-omics data to understand disease mechanisms and develop an AI-based risk scoring system. The interventions focus on using non-invasive imaging methods to screen and evaluate PVD comprehensively. During the study, participants will be monitored and assessed through imaging tests and clinical evaluations to measure major adverse cardiovascular events (MACE) and plaque characteristics over one year. Researchers will track the participants' cardiovascular health and disease progression using the collected imaging and biomarker data. The study requires participants to provide informed consent and follow scheduled evaluations to help build a full-cycle control information platform and risk warning model for PVD.
CONDITIONS
Official Title
An Imaging Study of Polyvascular Disease
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients with coronary artery disease showing 50% or more narrowing in any coronary artery on angiography
- Age 18 years or older
- Proposed use of OCT-IVUS integrated imaging system (for Task 1)
- Patients with coronary artery disease or with stroke or TIA confirmed by a neurologist (for Task 2)
- Able to provide written informed consent before any study procedures
You will not qualify if you...
- Severely tortuous or calcified coronary arteries making OCT-IVUS imaging difficult (Task 1)
- Uncontrolled congestive heart failure or acute left heart failure
- Claustrophobia
- Left main stem artery occlusion
- Planned coronary artery bypass grafting (CABG)
- Uncontrolled severe ventricular arrhythmia
- Active bleeding or severe bleeding tendency
- Acute stroke
- Hemodynamic instability or unstable cardiac electrical activity including shock
- Severe renal insufficiency or anuria unless dialysis is planned
- Contraindications to contrast media use
- Severe psychiatric or systemic illness causing poor cooperation
- Patients judged unsuitable for study participation by the investigator
- Inability to comply with follow-up schedule (Task 2)
- Life expectancy less than 6 months (Task 2)
AI-Screening
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Trial Site Locations
Total: 1 location
1
The Second Affiliated Hospital of Harbin Medical University
Harbin, Heilongjiang, China, 150000
Actively Recruiting
Research Team
M
Minghao Liu, MD.
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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