跳至主要内容
临床试验/NCT03939299
NCT03939299Unknown不适用

Optical Coherence Tomography Imaging Explores Long-term vasculAR Response and Healing profIle After successFul coronarY Stenting in Chronic Total Occlusion

Shanghai Zhongshan Hospital1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2019年4月15日最近更新:
适应症
干预措施

试验速览

阶段
不适用
发起方
入组人数
60
试验地点
1
主要终点
long-term stent thrombosis

研究概览

简要总结

True-false-true occurred during wire penetration in coronary CTO procedure. Subintimal stenting influences vascular response. Intravenous ultrasound confirmed wire position in the procedure. Then stenting procedure was performed. Optical coherence tomography was used for exploring long-term vascular response and healing profile after successful coronary stenting in CTO lesions.

详细描述

Chronic total occlusions (CTOs) are defined as coronary lesions with thrombolysis in myocardial infarction (TIMI) grade flow of 0 and present for more than 3 months. CTO is commonly recognized as the toughest lesion subset to be treated by percutaneous coronary interventions. With the remarkable progress in the technologies and techniques achieved in the PCI for CTO over the last decade, the rate of procedural success increased to 80-90%. Chronic total occlusion is associated with a higher incidence of malapposition and uncovered stent struts. At present, four strategies were used for CTO lesions, including: ante-grade wire escalation, ante-grade dissection reentry (ADR), retro-grade wire escalation, and retrograde dissection reentry (RDR). True-false-true occurred during wire penetration. Subintimal stenting influences vascular response. Intravenous ultrasound (IVUS) confirmed wire position in the procedure. Then stenting procedure was performed according to standard routine. Optical coherence tomography (OCT) was used for exploring long-term vascular response and healing profile after successful coronary stenting in CTO lesions.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •18~85 years old;
  • •Agree percutaneous coronary intervention without related contraindications;
  • •Chronic total occlusion confirmed by clinical and angiographic data, predicted high successful rate of stent implantation;
  • •Subjects (or legal guardians) understanding the testing requirements and procedures, and providing written informed consent.

排除标准

  • •Subjects associated with drugs allergy (such as contrast, sirolimus, or structure-related compounds fluorinated polymers, thienopyridine or aspirin);
  • •Subjects with active peptic ulcer, active gastrointestinal (GI) bleeding or other bleeding diathesis or coagulopathy;
  • •Subjects being suffered from other serious illness (such as cancer, congestive heart failure), which may cause drop in life expectancy to less than 12 months;
  • •Pregnant or breastfeeding women;
  • •Refused this trial;
  • •Subjects with severe liver or renal dysfunction (ALT >5×ULN,eGFR< 30ml/min/1.73mm2 or Scr>200 mmol/L);
  • •Active bleeding;
  • •Bleeding diathesis or coagulopathy, malignant tumors;
  • •Contraindication of anticoagulant drugs;
  • •Subjects with other situation not suitable for the study.

研究组 & 干预措施

OCT group

Experimental

Patients, whose coronary chronic total occlusion lesion was successfully implanted stent, received optical coherence tomography imaging immediately and at 9-12 months after index procedure.

干预措施: OCT (Procedure)

结局指标

主要结局

long-term stent thrombosis

时间窗: 9-12 month after index procedure

measured through OCT imaging result

long-term minimal stent area

时间窗: 9-12 month after index procedure

measured through OCT imaging result

long-term stent malapposition

时间窗: 9-12 month after index procedure

measured through OCT imaging result

immediately stent malapposition

时间窗: in the procedure

measured through OCT imaging result

long-term stent neointima

时间窗: 9-12 month after index procedure

measured through OCT imaging result

immediately minimal stent area

时间窗: in the procedure

measured through OCT imaging result

次要结局

  • Major Adverse Cardiovascular Events(9-12 month after index procedure)

研究者

发起方
Shanghai Zhongshan Hospital
申办方类型
Other
责任方
Sponsor

研究点 (1)

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