Treating Pulmonary Embolism With Laguna Thrombectomy System (TRUST)

Exclusion Criteria24

• Systolic pulmonary artery pressure > 70 mmHg on initial invasive hemodynamic assessments
• Life expectancy of < 90 days in the opinion of investigator at the time of enrollment
• Subject pregnant or breast feeding
• Current participation in another drug or medical device treatment study
• In active chemotherapy or radiation treatment for a malignancy during the course of the study
• Any intravascular administration of a fibrinolytic agent (such as Alteplase or Tenecteplase) within the last 30 days
• Presence of recently placed (<8 weeks) intracardiac devices (such as pacemaker leads) in the right ventricle or right atrium
• History of prior PE within the past 90 days
• FiO2 Requirement: > 40% (6 LPM) to keep oxygen saturation > 90%
• Hematocrit: < 28%
• Platelets: < 100,000/microliter
• Serum Creatinine: > 2 mg/dL
• International Normalized Ratio (INR): > 3
• Major Trauma Injury Severity Score (ISS): > 15
• Cardiovascular or pulmonary surgery within the last 7 days
• Known bleeding diathesis or coagulation disorder that cannot be managed with anti-coagulation
• History of known severe or chronic pulmonary arterial hypertension
• History or chronic left heart disease with left ventricular ejection fraction < 30%
• History of underlying lung disease that is oxygen dependent
• History of chest irradiation
• Known anaphylactic reaction to radiographic contrast agents that cannot be pretreated
• Any absolute contraindication to systemic or therapeutic dosage of heparin or anticoagulants
• Imaging or other evidence that suggests, in the opinion of the investigator, the subject is not appropriate for mechanical thrombectomy intervention (e.g., inability to navigate to target location, predominantly chronic clot or non-clot embolus)
• Known presence of clot in transit within right atrium or ventricle