drugset / Trial / NCT02604238

Efficacy and Safety of Half Dose Alteplase Added to Heparine, in Patients With Moderate Pulmonary Embolism

NCT02604238

RandomizedParallel-groupOpen-labelTreatment

Summary

The primary aim of this study is to evaluate whether mid dose (safe dose) of Alteplase in addition to standard treatment with heparin (LMWH) in patients with pulmonary embolism (PE) at intermediate risk, it is effective to reduce: * right ventricular dysfunction * pulmonary hypertension 24 hours and 7 days after the treatment * PE recurrence to 7days and 30 days after the treatment without increasing the incidence of bleeding intra-extracranial

Timeline

Start
2016-03
Primary completion
2016-03
Completion
2016-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Alteplase Protein / enzyme biologic 40 mg

Indications