A Prospective, Multicenter Study to Evaluate the Safety and Efficacy of an Aspiration Thrombectomy System in Acute Pulmonary Embolism
S
Sabah D. Butty, MD
Primary Investigator
Enrolling By Invitation
18 years - 100 years
All
Phase
N/A
1 participants needed
1 Location
Brief description of study
To evaluate the safety and efficacy of the Cleaner™ Pro Thrombectomy System for aspiration thrombectomy in patients with acute pulmonary embolism (PE).
THIS STUDY IS ENROLLING BY INVITATION ONLY
Detailed description of study
PRIMARY OUTCOMES:
- Change in Right Ventricle (RV)/Left Ventricle (LV) Ratio
- Rate of Major Adverse Events (MAEs)
SECONDARY OUTCOMES:
- Rate of device-related complications and device-related death
- Rate of device-related SAEs and all-cause mortality
- Rate of Symptomatic PE Recurrence
- Volume of blood aspirated
- Use of thrombolytics
- Change in Modified Miller Index
- Quality of Life assessed via PEmb-QoL
- Quality of Life assessed via EQ-5D-5L
Eligibility of study
You may be eligible for this study if you meet the following criteria:
- Conditions: Acute Pulmonary Embolism, Venous Thromboembolism, Cardiovascular Disease
-
Age: 18 years - 100 years
-
Gender: All
Inclusion Criteria:
- At least 18 years of age at the time of consent
- Clinical signs, symptoms, and presentation consistent with acute PE
- Onset of PE symptoms occurred within 14 days of presentation
- Filling defect in at least one main or lobar pulmonary artery evidenced by CTA
- RV dysfunction on CTA or echocardiography defined as RV/LV ratio >0.9
Exclusion Criteria:
- tPA use within 14 days prior to baseline CTA
- Systolic BP <90 mmHg for 15 min or the requirement of inotropic support to maintain systolic BP ≥90 mmHg
- Diagnosis of pulmonary hypertension or suspected undiagnosed pulmonary hypertension with peak PA >70 mmHg by right heart catheterization or elevated main pulmonary artery to aorta ratio (MPA:A)
- History of severe or chronic pulmonary hypertension
- FiO2 requirement >40% or >6 LPM to keep oxygen saturations >90%
- Hematocrit <28%
- Platelets <100,000/µL
- Serum creatinine >1.8 mg/dL
- INR >3
- aPTT (or PTT) >50 seconds on no anticoagulation
- History of heparin-induced thrombocytopenia (HIT)
- Recent (within six months) history of stroke, transient ischemic attack (TIA), or intracranial bleeding
- Recent (within one month) history of active bleeding from a major organ
- Absolute contraindication to anticoagulation
- Major trauma such as head trauma, or other active intracranial, or intraspinal disease within 14 days
- Morbidly obese (BMI >45 kg/m2) patient who by the judgement of the investigator is high risk for bleeding
- Presence of intracardiac lead in the right ventricle or right atrium placed within 6 months
- Cardiovascular or pulmonary surgery within last 7 days
- Cancer which requires active chemotherapy
- Known serious, uncontrolled sensitivity to radiographic agents
- Life expectancy <90 days, as determined by investigator
- Female who is pregnant
- Intracardiac thrombus
- Patients who present with cardiac arrest and/or are on extracorporeal membrane oxygenation (ECMO) or ECMO required to perform interventional procedure
- Simultaneous participation in another investigational study
- Patients with known coagulation disorders such as antiphospholipid, Protein C, and Protein S
- Presentation of PE with paradoxical emboli which may be diagnosed by concurrent stroke or concurrent arterialization
Updated on
28 Jul 2025.
Study ID: RADY-ARGON-CLEAN-PE, 27286
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