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Evaluation on the cHaracteristics of the true/false lumen and its prognostic value for coronary CTO patients just before stent implantation (LAOHUOJI): a CTO all-comer register study

Evaluation on the cHaracteristics of the true/false lumen and its prognostic value for coronary CTO patients just before stent implantation (LAOHUOJI): a CTO all-comer register study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100045967
Enrollment
Unknown
Registered
2021-04-30
Start date
2021-06-01
Completion date
Unknown
Last updated
2021-12-13

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

Conditions

Coronary atherosclerotic heart disease

Interventions

Case series:no

Sponsors

The Seventh People's Hospital of Zhengzhou
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Aged 18 to 80 years; 2.The duration of occlusion was more than 3 months; 3.The diameter of occluded vessels was more than or equal to 2.5mm; 4.Patients and their families refused surgical bypass surgery; 5.The subjects or their authorized family members voluntarily accepted the clinical trial and signed the written informed consent.

Exclusion criteria

Exclusion criteria: 1.Congenital heart disease, valvular heart disease, acute myocarditis, cardiomyopathy, pulmonary heart disease, bradyarrhythmia, such as atrioventricular block, sick sinus syndrome, etc; At the same time, they were complicated with malignant ventricular arrhythmias, such as persistent ventricular tachycardia; Patients with NYHA New York Heart function grade IV after standard treatment or left ventricular ejection fraction 700 x 10^9/L, white blood cell count < 3 x 10^9/L), Acute infectious diseases and autoimmune diseases; Malignant tumor, severe infection;, Severe nervous system diseases (severe disturbance of consciousness, severe nervous system infection, etc.), mental diseases (drug abuse, drug dependence, mental disorder can not cooperate) 4.The life expectancy is less than 12 months; 5. Pregnancy or planned pregnancy; 6.Aspirin, clopidogrel, ticagrelor and contrast media were intolerable; The patients could not tolerate dual antiplatelet therapy; 7.Participate in another drug or device study that has not yet reached the primary endpoint, or plan to participate in the clinical study within 12 months after the intervention.

Design outcomes

Primary

MeasureTime frame
IVUS based assessment of late lumen loss at 1-year follow-up;

Countries

China

Contacts

Public ContactZhao Yujie

The Seventh People's Hospital of Zhengzhou

lzyj74@126.com+86 18703677288

Outcome results

None listed

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