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临床试验/NCT01531829
NCT01531829Unknown4 期

Low Dose Rt-PA Plus LMWH Compared With LMWH Alone for the Treatment of Normotensive Pulmonary Embolism Patients With Acute RV Dysfunction: A Randomized,Multi-Center,Controlled Trial

Beijing Chao Yang Hospital35 个研究点 分布在 1 个国家目标入组 460 人开始时间: 2009年7月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
发起方
入组人数
460
试验地点
35
主要终点
the composite end point of death from any cause or treatment failure,recurrence of VTE

研究概览

简要总结

In selected patients with acute pulmonary embolism(PE), low dose (50mg/2h) recombinant tissue plasminogen activator (rt-PA) regimen had been reported to have less bleeding tendency than the FDA-approved rt-PA 100mg/2h regimen 100mg/2h regimen (3% vs.10%), it is worthwhile to reveal whether low dose rt-PA plus low molecular weight heparin (LMWH) can rapidly reverses RV pressure overload in PE, but not increase bleeding and other adverse events. The aim of the study is to compare thrombolytic treatment with LMWH in patients with acute normotensive PE with right ventricular dysfunction(RVD).

详细描述

In acute pulmonary embolism (PE), normotensive patients with acute RV dysfunction on echocardiography or computed tomography and with myocardial troponin elevation may have an adverse outcome. Thrombolysis rapidly reverses RV pressure overload in PE, but it increases the possibility of bleeding and it remains unclear whether it may improve the early or long-term clinical outcome of these selected normotensive patients.

In our previous study, we found that low dose (50mg/2h) recombinant tissue plasminogen activator (rt-PA) regimen had less bleeding tendency than the 100mg/2h regimen (3% vs.10%), it is worthwhile to reveal whether low dose rt-PA plus Low Molecular Weight Heparin (LMWH) can rapidly reverses RV pressure overload in PE, but not increase bleeding and other adverse events.

In this prospective, multicenter, randomized, control study, we compare low dose rt-PA plus LMWH vs. LMWH alone in acute normotensive pulmonary embolism patients with RV dysfunction. The primary efficacy outcome is the composite of death from any cause or treatment failure, improvements of right ventricular functions on echocardiogram and pulmonary artery obstruction on CT angiographs within 7 days of randomization. Second efficacy outcome is the recurrence of pulmonary embolism and deep venous thrombosis. Safety outcomes include serious life threatening bleeding such as cerebral hemorrhage and other major bleeding episodes, also include mild bleeding. In addition, 90-day clinical and echocardiographic follow-up will be performed, the recurrence of pulmonary embolism and deep venous thrombosis will be recorded. The study is expected to enroll approximately 460 patients.

By determining the benefits vs risks of Low dose rt-PA plus LMWH compared with LMWH alone for the treatment in submassive or intermediate-risk PE, this trial is expected to reveal the worth of Low dose rt-PA plus LMWH treatment and what kind of PE patients are suitable for thrombolysis.

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
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 18 y≤Age≤75y
  • Acute PE (first symptoms occurred 14 d or less before randomization) confirmed by lung scan, or a positive computed tomographic pulmonary angiogram, or a positive selective pulmonary angiogram
  • Hemodynamic stability, diastolic pressure>90mmHg.
  • RV dysfunction confirmed by echocardiography (≥1 criterion), except left-side heart disease, congenital heart disease and mitral valve disease.
  • Increase of the right ventricle showed presented with RV end-diastolic anteroposterior diameter >25 mm, Right/left ventricular end-diastolic diameter >1 (apical or subcostal 4-chamber view) or Right/left ventricular end-diastolic anteroposterior diameter >0.5
  • Hypokinesis of RV-free wall (range of motion less than 5 mm)
  • Tricuspid regurgitation pressure >30mmHg

排除标准

  • RV anterior wall thickness > 5mm confirmed by echocardiography
  • Active internal bleeding and spontaneous intracranial hemorrhage in preceding 6 months
  • Major surgery, organ biopsy or non-compressible punctures within 2 weeks
  • Ischemic stroke occurred within 2 months
  • Gastrointestinal bleeding within 10 days
  • Severe trauma occurred within15 days
  • Neurosurgery or eye surgery within 1 months
  • Severe hypertension difficult to control (systolic blood pressure>180mmHg or diastolic blood pressure>110mmHg)
  • Cardiopulmonary resuscitation
  • Platelet count less than 100×109 / L
  • Pregnancy, or within 2 week post partum
  • Infective endocarditis; left atrial thrombus; aneurysm
  • Serious liver and kidney dysfunction
  • Diabetic hemorrhagic retinopathy
  • Suffering with bleeding disorders
  • Chronic thromboembolic pulmonary hypertension
  • Moderate to severe chronic obstructive pulmonary disease (COPD).

研究组 & 干预措施

Low dose (50mg/2h) rt-PA plus LMWH

Experimental

Low dose (50mg/2h) recombinant tissue plasminogen activator (rt-PA) plus low molecular weight heparin(LMWH)regimen

干预措施: Recombinant tissue plasminogen activator (rt-PA) (Drug)

LMWH

Active Comparator

Low molecular weight heparin

干预措施: Low Molecular Weight Heparin (Drug)

结局指标

主要结局

the composite end point of death from any cause or treatment failure,recurrence of VTE

时间窗: 7 days

improvements of right ventricular functions on echocardiogram and pulmonary artery obstruction on CT angiographs

时间窗: 7 days

clinical relevant non-major bleedings

时间窗: 7 days

serious life threatening bleeding such as cerebral hemorrhage and other major bleeding episodes

时间窗: 7 days

次要结局

  • the composite end point of death from any cause or treatment failure,recurrence of VTE(3 months and 6 months)
  • improvements of right ventricular functions on echocardiogram and pulmonary artery obstruction on CT angiographs(3 months and 6 months)
  • serious life threatening bleeding such as cerebral hemorrhage and other major bleeding episodes(3 months and 6 months)
  • clinical relevant non-major bleedings(3 months and 6 months)

研究者

发起方
Beijing Chao Yang Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Chen WANG

Professor of respiratory and critical care medicine

Beijing Chao Yang Hospital

研究点 (35)

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