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临床试验/NCT03886194
NCT03886194Unknown不适用

Comparative Study of Interventional and Systemic Thrombolysis in Patients With High-risk and High-risk Pulmonary Embolism

First Affiliated Hospital Xi'an Jiaotong University1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2019年8月18日最近更新:
适应症

试验速览

阶段
不适用
入组人数
40
试验地点
1
主要终点
Right heart load

研究概览

简要总结

Pulmonary embolism (PE) is a pulmonary vascular disease that seriously endangers human health. It has the characteristics of high morbidity, high mortality, high misdiagnosis rate and low detection rate. The mortality rate in March is about 10%. The high-risk and high-risk PE mortality rate is greater than 15%. Chronic thromboembolic pulmonary hypertension (CTEPH) is a serious sequelae after PE, with a poor prognosis and expensive treatment. Systemic thrombolysis is the preferred treatment for acute high-risk pulmonary embolism, which can reduce mortality, but the incidence of major bleeding is increased by 5 times and hemorrhagic stroke is increased by 10 times. Recent studies have concluded that interventional therapy is a viable approach with a high success rate, effective improvement of clinical outcomes, and minimization of major bleeding risks. However, there is no good prospective study of interventional therapy compared with systemic thrombolytic therapy. This study was enrolled in the diagnosis of high-risk and high-risk PE patients, randomized to the system of thrombolytic therapy or interventional therapy (including pulmonary artery catheter contact thrombolysis, catheter thrombectomy, thrombus aspiration and mechanical thrombectomy, etc.) Symptoms improved during surgery, right heart condition, mortality and complications, and were followed up to December to observe PE recurrence CETPH, survival and cardiopulmonary function. In order to provide new evidence for the treatment of fatal pulmonary embolism.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

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

入选标准

  • Han population with age greater than or equal to 14 years old and less than or equal to 85 years;
  • Signed informed consent;
  • confirmed initial acute pulmonary embolism, within 2 weeks of disease, pulmonary embolism confirmed methods include: CTA/DSA/pulmonary ventilation Imaging: confirmed as at least 1 trunk pulmonary artery or proximal low lobe artery filling defect;
  • risk stratification for intermediate high-risk or high-risk pulmonary embolism: 2014ESC stratified definition of high-risk and high-risk: high-risk PE: hemodynamics Obstruction, systolic blood pressure <90mmHg, greater than 15 minutes; medium and high risk PE: right ventricular dysfunction imaging findings (RV / LV ≥ 0.9) and myocardial damage indicators positive (TNT > 0.1 ng / ml);
  • blood flow at admission The kinetics are stable.

排除标准

  • patients with mental illness can not cooperate with the completion of the study; -CTPA / DSA contraindications patients;
  • any contraindications listed in the instructions for treatment of the drug involved in the study;
  • diseases associated with coagulopathy leading to the risk of clinically relevant bleeding;
  • There are active bleeding or high risk of bleeding in patients with anticoagulant thrombolysis contraindications;
  • creatinine clearance rate <30 mL / min;
  • life expectancy ≤ 6 months;
  • childbearing age or pregnancy, lactation period without appropriate contraceptive measures Subjects;
  • participated in any other drug or medical device study within 30 days prior to randomization;
  • cases that the investigator considered unsuitable for participation in the trial.

结局指标

主要结局

Right heart load

时间窗: 30 days

RV/LV (thoracic enhanced CT/cardiac ultrasound),pulmonary artery pressure (catheter/cardiac ultrasound),troponin T, NT-proBNP, 6-minute walk test

death within 30 days

时间窗: 30 days

number of deaths

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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