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Development of risk prediction model for long-term adverse cardiovascular events in patients with left main disease

An exploratory study of risk prediction model for long-term adverse cardiovascular events in patients with left main disease after IVUS-guided PCI

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500100941
Enrollment
Unknown
Registered
2025-04-17
Start date
2022-08-06
Completion date
Unknown
Last updated
2025-04-21

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

Conditions

Complex left main coronary artery disease

Interventions

Subjects With MACCE and Subjects Without MACCE:NA

Sponsors

Wuhan Asia Heart Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.The patient must be >=18 years of age; 2.The patient has a lesion of >= 50% in the left main coronary artery, along with clear indications for PCI suggested by the treating interventionalist; 3.The patient is willing to undergo percutaneous coronary intervention (PCI) guided by intravascular ultrasound (IVUS). 4.Silent ischemia, stable angina, unstable angina, non-ST-segment elevation MI (NSTEMI), ST-segment elevation MI (STEMI); 5.Able to understand and provide informed consent and comply with all study procedures.

Exclusion criteria

Exclusion criteria: 1.Female patients who are pregnant or nursing; 2.cardiogenic shock; 3.Prior PCI of the LM at any time prior to enrollment; 4.Patients unable to tolerate, obtain or comply with dual antiplatelet therapy for at least 6 months in stable patients and 1 year in ACS patients; 5.Complicated with severe hepatic insufficiency or renal insufficiency. 6.Complicated with severe coagulation abnormalities. 7.Complicated with malignant tumors. 8.Non-cardiac co-morbidities with a life expectancy less than 1 years; 9.Currently participating in another trial that is not yet at its primary outcome; the patient is not allowed to participate in another investigational device or drug study for at least 12 months after enrollment;

Design outcomes

Primary

MeasureTime frame
Composite endpoint: major adverse cardiac and cerebrovascular event (MACCE) include cardiac death, myocardial infarction, target vessel revascularization, non - fatal stroke;

Countries

China

Contacts

Public ContactHua Yan

Wuhan Asia Heart Hospital

yanhua0807@aliyun.com+86 27 65796888

Outcome results

None listed

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