At a glance
ClinicalIndex Comparison RecordN/ACompleted· 10 enrolled
Drug / intervention
Vertex Pulmonary Embolectomy Systemdevice
Likely dose
Vertex Pulmonary Embolectomy System (mechanical device; no dose applicable)AI-extracted
Key inclusion· 5
- ✓Age 18 to <80 years
- ✓Acute PE symptoms onset ≤14 days
- ✓CTA evidence of proximal PE (filling defect in main or interlobar pulmonary artery)
- ✓RV/LV ratio >0.9 on CTA indicating right ventricular strain
Key exclusion· 31
- ✕Thrombolytic use within 30 days
- ✕Pulmonary artery pressure >70 mmHg on right heart catheterization
- ✕Vasopressor requirement after fluids to maintain SBP ≥90 mmHg
- ✕Heart rate >130 bpm prior to procedure
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Selective Pulmonary-artery Intervention to Reduce Acute Right-heart tEnsion-I
In Brief
A clinical study evaluating Vertex Pulmonary Embolectomy System for Pulmonary Embolism. Completed, enrolled 10 participants across 2 sites in 2 countries.
Detailed Summary
This study study is a prospective, single-arm, multicenter study to evaluate the safety and effectiveness of the Vertex Pulmonary Embolectomy System in participants presenting with clinical signs and symptoms of pulmonary embolism.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsPulmonary Embolism
CountriesAustria, Poland
Collaborators--
Timeline
N/ACompletedFinished
20252026
First PostedAug 2024
Enrollment StartSep 2024
Primary CompletionApr 2025
Study CompletionMay 2025
TodayJul 2026
First PostedAug 26, 2024
Enrollment StartSep 10, 2024
Primary CompletionApr 24, 2025
Study CompletionMay 21, 2025
TodayJul 2, 2026
Enrollment to primary: 7 monthsPosted 1.8 years ago
Interventions
Vertex Pulmonary Embolectomy Systemdevice
Use of Vertex Pulmonary Embolectomy System to treat pulmonary embolism.