Ignite Creation Date:
2025-12-25 @ 2:12 AM
Ignite Modification Date:
2025-12-27 @ 12:57 PM
Study NCT ID:
NCT06571760
Status:
COMPLETED
Last Update Posted:
2025-05-29
First Post:
2024-08-23
Is NOT Gene Therapy:
True
Has Adverse Events:
False
Brief Title:
Selective Pulmonary-artery Intervention to Reduce Acute Right-heart tEnsion-I
Sponsor:
Organization:
Raw JSON
{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'conditionBrowseModule': {'meshes': [{'id': 'D011655', 'term': 'Pulmonary Embolism'}, {'id': 'D016769', 'term': 'Embolism and Thrombosis'}, {'id': 'D004617', 'term': 'Embolism'}, {'id': 'D002318', 'term': 'Cardiovascular Diseases'}], 'ancestors': [{'id': 'D008171', 'term': 'Lung Diseases'}, {'id': 'D012140', 'term': 'Respiratory Tract Diseases'}, {'id': 'D014652', 'term': 'Vascular Diseases'}]}}, 'protocolSection': {'designModule': {'phases': ['NA'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'NA', 'maskingInfo': {'masking': 'NONE'}, 'primaryPurpose': 'TREATMENT', 'interventionModel': 'SINGLE_GROUP'}, 'enrollmentInfo': {'type': 'ACTUAL', 'count': 10}}, 'statusModule': {'overallStatus': 'COMPLETED', 'startDateStruct': {'date': '2024-09-10', 'type': 'ACTUAL'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2025-05', 'completionDateStruct': {'date': '2025-05-21', 'type': 'ACTUAL'}, 'lastUpdateSubmitDate': '2025-05-27', 'studyFirstSubmitDate': '2024-08-23', 'studyFirstSubmitQcDate': '2024-08-23', 'lastUpdatePostDateStruct': {'date': '2025-05-29', 'type': 'ACTUAL'}, 'studyFirstPostDateStruct': {'date': '2024-08-26', 'type': 'ACTUAL'}, 'primaryCompletionDateStruct': {'date': '2025-04-24', 'type': 'ACTUAL'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'Reduction in Right ventricle (RV) / Left Ventricle (LV) ratio', 'timeFrame': 'From baseline to 48 hours or discharge', 'description': 'Reduction in RV/LV ratio from baseline to 48 hours or discharge by (core lab assessed) CT angiography'}, {'measure': 'Major Adverse Events (AEs), a composite of:', 'timeFrame': 'Within 48 hours of procedure', 'description': 'Device-related death within 48 hours\n\nMajor bleeding within 48 hours\n\nDevice-related AEs within 48 hours, including:\n\n* Clinical deterioration\n* Pulmonary vascular injury\n* Cardiac injury'}]}, 'oversightModule': {'isUsExport': True, 'oversightHasDmc': False, 'isFdaRegulatedDrug': False, 'isUnapprovedDevice': True, 'isFdaRegulatedDevice': True}, 'conditionsModule': {'keywords': ['Embolism and Thrombosis', 'Pulmonary Embolism', 'Embolism', 'Cardiovascular Diseases'], 'conditions': ['Pulmonary Embolism']}, 'descriptionModule': {'briefSummary': '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.', 'detailedDescription': 'The 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 acute pulmonary embolism.\n\nThe Vertex Pulmonary Embolectomy System is intended for the non-surgical removal of emboli and thrombi from blood vessels as a means for treating pulmonary embolism.'}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['ADULT', 'OLDER_ADULT'], 'maximumAge': '79 Years', 'minimumAge': '18 Years', 'healthyVolunteers': False, 'eligibilityCriteria': 'Inclusion Criteria:\n\n1. Age ≥ 18 years \\< 80 years\n2. Acute onset of symptoms ≤ 14 days consistent with the presence of pulmonary embolism.\n3. CTA evidence (site determined) of proximal PE (filling defect in at least one main or interlobar pulmonary artery)\n4. RV/LV ratio of \\> 0.9 on CTA as assessed by investigator (site determined).\n5. Systolic blood pressure ≥ 90 mmHg (initial SBP may be ≥ 80 mmHg if the pressure recovers to ≥ 90 mmHg with fluids)\n6. Subject is willing and able to provide written informed consent prior to receiving any non-standard of care clinical investigation plan specific procedures\n7. Subject is willing and able to comply with all clinical investigation plan required follow-up visits\n\nExclusion Criteria:\n\n1. Thrombolytic use within 30 days of baseline CTA\n2. Pulmonary hypertension with peak pulmonary artery pressure \\> 70 mmHg by right heart catheterization (site determined)\n3. Vasopressor requirement after fluids to keep pressure ≥ 90 mmHg\n4. Unstable heart rate \\> 130 beats per minute prior to procedure\n5. FiO2 requirement \\> 40% or \\> 6 LPM to keep oxygen saturation \\> 90%\n6. Hematocrit \\< 28%\n7. Platelets \\< 100,000/µL\n8. Serum baseline creatinine \\> 1.8 mg/dL\n9. International normalized ratio (INR) \\> 3\n10. Major trauma injury severity score (ISS) \\> 15 within the past 14 days\n11. Presence of intracardiac lead in the right ventricle or right atrium placed \\<180 days prior to the index procedure\n12. Cardiovascular or pulmonary surgery within last 30 days\n13. Actively progressing cancer requiring chemotherapy\n14. Known bleeding diathesis or coagulation disorder\n15. Left bundle branch block\n16. History of severe or chronic pulmonary arterial hypertension\n17. History of chronic left heart disease with left ventricular ejection fraction ≤ 30%\n18. History of decompensated heart failure\n19. Patients on extracorporeal membrane oxygenation (ECMO)\n20. History of underlying lung disease that is oxygen dependent\n21. History of chest irradiation\n22. History of heparin-induced thrombocytopenia (HIT)\n23. Contraindication to systemic or therapeutic doses of heparin or anticoagulants\n24. Known anaphylactic reaction to radiographic contrast agents that cannot be pretreated\n25. Imaging evidence or other evidence that suggests, in the opinion of the Investigator, the Subject is not appropriate for mechanical thrombectomy intervention\n26. Life expectancy of \\< 365 days, as determined by Investigator\n27. Female who is pregnant or nursing\n28. Current participation in another investigational drug or device treatment study\n29. Inability to lay flat for procedure\n30. Known presence of right-to-left cardiac shunt\n31. History of Hemorrhagic or Ischemic Stroke, including Transient Ischemic Attack, within last 90 days\n32. Current or history of chronic thromboembolic pulmonary hypertension (CTEPH) or chronic thromboembolic disease (CTED) diagnosis'}, 'identificationModule': {'nctId': 'NCT06571760', 'acronym': 'SPIRARE I', 'briefTitle': 'Selective Pulmonary-artery Intervention to Reduce Acute Right-heart tEnsion-I', 'organization': {'class': 'INDUSTRY', 'fullName': 'Neptune Medical'}, 'officialTitle': 'Selective Pulmonary-artery Intervention to Reduce Acute Right-heart tEnsion-I', 'orgStudyIdInfo': {'id': 'CSP-01'}}, 'armsInterventionsModule': {'armGroups': [{'type': 'EXPERIMENTAL', 'label': 'Vertex Pulmonary Embolectomy System', 'description': 'Patients presenting with clinical signs and symptoms of acute pulmonary embolism and who meet the study criteria will be treated with the Vertex Pulmonary Embolectomy System', 'interventionNames': ['Device: Vertex Pulmonary Embolectomy System']}], 'interventions': [{'name': 'Vertex Pulmonary Embolectomy System', 'type': 'DEVICE', 'description': 'Use of Vertex Pulmonary Embolectomy System to treat pulmonary embolism.', 'armGroupLabels': ['Vertex Pulmonary Embolectomy System']}]}, 'contactsLocationsModule': {'locations': [{'zip': '1090', 'city': 'Vienna', 'country': 'Austria', 'facility': 'AKH Vienna - Medical university of Vienna', 'geoPoint': {'lat': 48.20849, 'lon': 16.37208}}, {'city': 'Krakow', 'country': 'Poland', 'facility': 'Jagiellonian University', 'geoPoint': {'lat': 50.06143, 'lon': 19.93658}}], 'overallOfficials': [{'name': 'Aadi Chachad', 'role': 'STUDY_DIRECTOR', 'affiliation': 'Sponsor GmbH'}]}, 'ipdSharingStatementModule': {'ipdSharing': 'NO', 'description': 'Will not be sharing IPD.'}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'Neptune Medical', 'class': 'INDUSTRY'}, 'responsibleParty': {'type': 'SPONSOR'}}}}