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Research on an intelligent planning system for coronary interventional surgery that integrates 'anatomy and function' CTA images

Research on an intelligent planning system for coronary interventional surgery that integrates 'anatomy and function' CTA images

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500102316
Enrollment
Unknown
Registered
2025-05-13
Start date
2025-07-01
Completion date
Unknown
Last updated
2025-05-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Coronary Disease

Interventions

Intervention group:One-Stop CTA imaging guidance for coronary intervention
Control Group:Traditional coronary intervention surgery process

Sponsors

Senior Department of Cardiology, the Sixth Medical Centre, Chinese PLA General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Age>=18 years old and=70% or 50-69%, and significant ischemia as assessed by CTA functional evaluation. Coronary intervention surgery is planned for treatment; 3. There is only one target lesion in the target vessel; 4. The patient and their family agree to participate in this clinical study and undergo regular postoperative follow-up, and sign a written informed consent form.

Exclusion criteria

Exclusion criteria: 1. There are contraindications for coronary angiography or coronary CTA, including known severe iodine contrast agent allergy, uncontrolled hyperthyroidism, pregnancy or lactation, high risk of contrast agent nephropathy, etc; 2. Hemodynamic or clinical instability, systolic blood pressure38mm, diameter>4mm, severe calcification, severe vessel distortion, bifurcation, and left main trunk lesions; 7. Poor quality of coronary CTA images affects diagnosis and subsequent functional evaluation (<=Likert level 3); 8. The patient is participating in another clinical study of a drug or medical device whose primary endpoint has not yet been evaluated.

Design outcomes

Primary

MeasureTime frame
The total time required for coronary intervention treatment of target lesions in a single vessel;Residual stenosis degree;Intraoperative complications;

Secondary

MeasureTime frame
Major adverse cardiovascularand cerebrovascular events (MACCE);In-stent restenosis;Fluoroscopy Time;Time required for stent implantation;The total cost of cardiovascular-related examinations upon admission;

Countries

China

Contacts

Public ContactJun Guo

Senior Department of Cardiology, the Sixth Medical Centre, Chinese PLA General Hospital

guojun301@126.com+86 188 1306 5025

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026