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临床试验/NCT04965207
NCT04965207尚未招募不适用

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

Shanghai 10th People's Hospital0 个研究点目标入组 1,000 人开始时间: 2021年10月1日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
1,000
主要终点
Late Lumen Loss

研究概览

简要总结

IVUS will be used to evaluate the ratio of false lumen to occluded segment, the ratio of false lumen to stent length, the location characteristics of false lumen and its prognostic value for perioperative complications, 1-year late lumen loss and MACCE events in patients with coronary CTO.

详细描述

At present, novel technologies of CTO interventional therapy become mature. These technologies usually artificially cause dissection of coronary artery. The events such as collateral vessel loss, vascular injury and tear, perforation, pericardial tamponade caused by false lumen may theoretically affect the perioperative and long-term prognosis of patients. In this study, intravascular ultrasound (IVUS) was used to evaluate the characteristics of true lumen and false lumen in CTO segment, so as to determine its impact on the prognosis of patients.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Prospective

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •18 to 80 years old;
  • •be diagnosed with CTO;
  • •CTO located in an epicardial coronary artery with a reference diameter of ≥ 2.5mm;
  • •comply with all the evaluations and follow-up protocols.

排除标准

  • •suffered from acute myocardial infarction within the previous 3 months;
  • •rheumatic valvular disease;
  • •severe arrhythmia;
  • •lesions unsuitable for PCI;
  • •severely abnormal hematopoietic systems, such as platelet counts <100*10^9/L or > 700*10^9/L and white blood cell counts < 3*10^9/L;
  • •with active bleeding or bleeding tendencies(active ulcers, short-term ischemic stroke, history of hemorrhagic stroke, intracranial space occupying lesions, recent craniocerebral trauma, and other bleeding or bleeding tendency);
  • •severe coexisting conditions, including severe renal function dysfunction [Glomerular filtration rate less than 60ml/min • 1.73 m2), severe hepatic dysfunction [glutamic-pyruvic transaminase (ALT) or glutamic-oxal acetic transaminase (ALT) elevated more than three times that of the upper limit of the normal reference], severe heart failure (NYHA classification III-IV), acute infectious diseases and immune disorders; tumors; surgery within 3 months;
  • •a life expectancy less than 12 months;
  • •pregnancy or planning to become pregnant;
  • •history of allergy or adverse reactions to aspirin, clopidogrel, ticagrelor, stains, contrast material, anticoagulant, or stents;
  • •cannot tolerate dual antiplatelet treatment;
  • •unable to communicate due to cognitive impairment, auditory, or visual impairment;
  • •participating in another trial for medication or an apparatus and in which the main endpoint has not been reached, or plan to participate in a clinical trial within 12 months of the intervention.

结局指标

主要结局

Late Lumen Loss

时间窗: 1 year after PCI

Late Lumen Loss was defined as the difference between post-stenting minimal lumen diameter (MLD) minus MLD at the time of follow-up.

次要结局

  • Late Lumen Loss(3 year after PCI)
  • Major Adverse of Cardiovascular and Cerebrovascular Events(MACCE)(Within the first week after PCI, at the 1-year follow-up and at the 3-year follow-up)
  • Complications(Within the first week after PCI)

研究者

发起方
Shanghai 10th People's Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Ya-Wei Xu

Chief physician

Shanghai 10th People's Hospital

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