跳至主要内容
临床试验/NCT02238639
NCT02238639已完成不适用

Efficacy and Safety of an Active Strategy for the Diagnosis and Treatment of Acute Pulmonary Embolism (PE) in Patients With Unexplained Exacerbations of Chronic Obstructive Pulmonary Disease (COPD): a Randomized Clinical Trial

Ministry of Health, Spain20 个研究点 分布在 1 个国家目标入组 746 人开始时间: 2014年10月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
746
试验地点
20
主要终点
All-cause Mortality, Symptomatic Venous Thromboembolism Recurrence, or Need for Readmission.

研究概览

简要总结

The primary objective is to demonstrate the clinical benefits of an active strategy for the diagnosis and treatment of PE compared to usual care in patients with unexplained exacerbations of COPD who require hospital admission.

The secondary objective is to assess the safety of an active strategy for the diagnosis and treatment of PE compared to usual care in patients with unexplained exacerbations of COPD who require hospital admission.

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 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Confirmation of COPD according to SEPAR-ALT criteria: post-bronchodilator forced expiratory volume in one second (FEV1)/forced vital capacity (FVC) < 0.7;
  • Hospital admission because COPD exacerbation without initial clinical suspicion of PE in the Emergency Department (according by the Emergency Department physician evaluation).

排除标准

  • Contraindication to multidetector computed tomographic angiography (allergy to intravenous contrast medium, or renal failure defined as a creatinine clearance less than 30 mL/min, according to the Cockcroft-Gault formula)
  • Informed consent denied
  • Pregnancy
  • Life expectancy less than 3 months
  • Anticoagulant therapy at the time of hospital admission
  • Diagnosis of pneumothorax, or pneumonia (fever, and purulent sputum, and new infiltrate in chest X-ray)
  • Diagnosis of lower respiratory tract infection (fever [>37.8ºC], increased sputum volume and/or increased sputum purulence).
  • Indication of invasive mechanical ventilation at the time of hospital admission;
  • Impossibility for follow-up.

结局指标

主要结局

All-cause Mortality, Symptomatic Venous Thromboembolism Recurrence, or Need for Readmission.

时间窗: 90-day follow-up

Clinical composite endpoint of all-cause mortality, or symptomatic venous thromboembolism recurrence, or need for readmission.

次要结局

  • Serious Adverse Events(90-day follow-up)
  • Hospitalization(90-day follow-up)
  • Major Bleeding(90-day follow-up)
  • Clinically Relevant Non Major Bleeding(90-day follow-up)
  • All-cause Mortality(90-day follow-up)
  • Symptomatic Recurrent Venous Thromboembolism(90-day follow-up)

研究者

发起方
Ministry of Health, Spain
申办方类型
Other Gov
责任方
Principal Investigator
主要研究者

David Jimenez

Senior Consultant

Ministry of Health, Spain

研究点 (20)

Loading locations...

相似试验