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Interventional Strategy Selection and Prognosis Analyses of Coronary Chronic Total Occlusion Guiding by Intravascular Imaging

Interventional Strategy Selection and Prognosis Analyses of Coronary Chronic Total Occlusion Guiding by Intravascular Imaging

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000035615
Enrollment
Unknown
Registered
2020-08-15
Start date
2021-01-01
Completion date
Unknown
Last updated
2020-08-31

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

Conditions

Coronary Artery Disease

Interventions

Case series:Nil

Sponsors

Zhongshan Hospital Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 85 years; 2. Patients who agree to receive PCI treatment and have no relevant treatment contraindication; 3. Patients with CTO lesion suggested by coronary angiography, with expected high success rate of surgery and planned to receive stent implantation after vascular patency; 4. Have independent civil capacity, agree to be included in this clinical study and follow-up, and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. The patient is allergic to contrast agent and other related drugs; 2. Recent history of bleeding tendency, active gastrointestinal ulcer, cerebral hemorrhage or arachnoid hemorrhage, stroke within half a year, antiplatelet agents and anticoagulant therapy contraindication can not be anticoagulant therapy; 3. Other diseases may affect the life expectancy of less than 12 months; 4. Pregnant or lactating; 5. Patients refuse to participate in the study. 6. Severe liver and kidney dysfunction (ALT > 5 ULN, eGFR 200 mmol/L); 7. Active bleeding; 8. Known bleeding disorders or malignant tumor diseases; 9. Patients with contraindications to the use of antithrombotic drugs; 10. Patients who are not suitable for this study in the opinion of the investigator.

Design outcomes

Primary

MeasureTime frame
Minimum Stent Area;Stent Plaque Prolapse and Thrombus;Neointimal thickness;Stent thrombosis;Stent malapposition;Effective area;Edge dissection;

Countries

China

Contacts

Public ContactQian Juying

Zhongshan Hospital, Fudan University

qian.juying@zs-hospital.sh.cn+86 13661813201

Outcome results

None listed

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