EUCTR2014-003273-42-FR进行中(未招募)1 期
Comparing a diuretic vascular filling in the initial management of acute pulmonary embolism with right ventricular dysfunction normotensive
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中(未招募)
- 发起方
- CHU de Nice
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •older than 18 Patient
- •Hospitalized in the first 24 hours of a serious EP normotensive formally diagnosed (by a chest CT)
- •The serious nature without hypotension is defined by the presence of:
- •- From biological criteria: troponin and / or BNP positive
- •- In sonographic criteria: dilated right ventricle defined by echocardiography right over left ventricle ratio (VG)> 0.9 in apical 4-chamber or 0.7 in large parasternal axis and right ventricular systolic dysfunction (TAPSE <16 mm and S 'pulsed TDI tricuspid <10 cm / sec) or pulmonary arterial hypertension (PAH) Pulmonary Arterial Pressure with systolic (PAPs)> 35 mmHg or paradoxical septum
- •Informed consent signed
- •Affiliation to social security
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 30
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 30
排除标准
- •Thrombolysis before inclusion
- •State of cardiogenic shock defined as systolic BP <90 mmHg or a drop of> 40 mmHg in systolic BP for> 15 minutes
- •severe chronic renal impairment defined by clearance <30 ml / min.
- •pregnant or nursing woman (a pregnancy test will be performed for women of childbearing age and the results will be communicated to the patient by a doctor of his choice)
- •Most People under guardianship
- •hospitalized without their consent and not protected by law No
- •Private person of liberty
- •Residence time of more than 24 hours in another department after the positive diagnosis of pulmonary embolism
研究者
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