[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Akura Medical\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":79},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,39,60],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":17,"targetDuration":4,"studyType":20,"phases":21,"briefSummary":23,"conditions":24,"keywords":4,"overallStatus":26,"whyStopped":4,"lastUpdateSubmitDate":27,"lastUpdatePostDateStruct":28,"startDateStruct":31,"completionDateStruct":33,"leadSponsor":35,"locationsCount":38},"100567770","safety-and-effectiveness-of-the-akura-thrombectomy-system-for-use-in-the-removal-of-emboli-from-the-pulmonary-arteries-in-treating-acute-pulmonary-embolism-pe-100567770",false,"NCT06672510","Safety and Effectiveness of the Akura Thrombectomy System for Use in the Removal of Emboli From the Pulmonary Arteries in Treating Acute Pulmonary Embolism (PE)","Inclusion Criteria:\n\n* The patient is 18 years of age or older and deemed medically eligible for interventional procedure, per institutional guidelines and clinical judgement\n* Clinical signs, symptoms and presentation consistent with acute PE\n* PE symptom duration ≤ 14 days\n* CTA evidence of proximal PE (filling defect in at least one main or lobar pulmonary artery)\n* CTA evidence of RV\u002FLV ratio of ≥ 0.9 (NOTE: Enrollment qualification assessment is based on the Investigator's interpretation of RV\u002FLV ratio at baseline)\n* Systolic BP ≥ 90 mmHg (initial SBP may be \\\u003C 90 mmHg but ≥ 80 mmHg if the pressure recovers with volume resuscitation)\n* Stable HR \\\u003C 130 BPM prior to the procedure\n\nExclusion Criteria:\n\n* Prior PE \\\u003C180 days from index procedure\n* Thrombolytic use within 30 days prior to baseline CTA\n* Pulmonary hypertension with peak pulmonary arterial pressure (PAP) \\> 70 mmHg by right heart catheterization\n* Vasopressor requirement after fluids to keep pressure at ≥ 90 mmHg\n* FiO2 requirement \\> 40% or \\> 6 LPM (to keep oxygen saturation \\> 90%)\n* Hematocrit \\\u003C 28% (Note: hematocrit required within 6 hrs. of index procedure)\n* Platelets \\\u003C 100,000\u002FμL\n* eGFR \\\u003C30 ml\u002Fmin per 1.73 m2\n* International normalized ratio (INR) \\> 3\n* Major trauma injury severity score (ISS) \\> 15\n* Presence of intracardiac lead in right ventricle or atrium placed ≤ 6 months of enrollment\n* Cardiovascular or pulmonary surgery within the last 7 days\n* Actively progressing cancer treated by chemotherapeutics\n* Known bleeding diathesis or coagulation disorder\n* Left bundle branch block\n* History of severe or chronic pulmonary arterial hypertension\n* History of chronic left heart disease with left ventricular ejection fraction ≤ 30%\n* History of uncompensated heart failure.\n* History of underlying lung disease that is oxygen dependent\n* History of chest irradiation\n* History of heparin-induced thrombocytopenia (HIT)\n* Contraindication to systemic or therapeutic doses of anticoagulants\n* Known anaphylactic reaction to radiographic contrast agents that cannot be pretreated\n* Known residual iliac deep vein thrombosis (DVT), inferior vena cava (IVC) clot or clot in transit (right atrium and\u002For right ventricle)\n* CTA imaging or other evidence that suggest, 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)\n* Life expectancy \\\u003C 90 days, as determined by investigator (e.g., stage 4 cancer, frailty or severe COVID infections)\n* Female who is pregnant or nursing\n* Current participation in another investigational drug or device treatment study","ALL","18 Years",{"count":18,"type":19},118,"ESTIMATED","INTERVENTIONAL",[22],"NA","This study is a prospective, single-arm, interventional, multicenter study to evaluate the safety and effectiveness of percutaneous mechanical thrombectomy using the Akura Thrombectomy System in subjects with acute pulmonary embolism (PE).",[25],"Pulmonary Embolism Acute","RECRUITING","2025-12-11",{"date":29,"type":30},"2025-12-17","ACTUAL",{"date":32,"type":30},"2025-01-01",{"date":34,"type":19},"2026-12",{"name":36,"class":37},"Akura Medical","INDUSTRY",12,{"id":40,"slug":41,"hasResults":11,"nctId":42,"briefTitle":43,"officialTitle":43,"acronym":4,"eligibilityCriteria":44,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":45,"enrollmentInfo":46,"targetDuration":4,"studyType":20,"phases":48,"briefSummary":49,"conditions":50,"keywords":4,"overallStatus":26,"whyStopped":4,"lastUpdateSubmitDate":51,"lastUpdatePostDateStruct":52,"startDateStruct":54,"completionDateStruct":56,"leadSponsor":58,"locationsCount":59},"100543980","safety-and-effectiveness-of-the-akura-thrombectomy-system-in-the-treatment-of-acute-pulmonary-embolism-100543980","NCT06362928","Safety and Effectiveness of the Akura Thrombectomy System in the Treatment of Acute Pulmonary Embolism","Inclusion Criteria:\n\n1. Patient is \\> 18 and \\\u003C 90 years old\n2. Clinical signs and symptoms consistent with acute PE\n3. PE symptom duration ≤ 14 days\n4. CTA evidence of proximal PE (filling defect in at least one main or lobar pulmonary artery as determined by the investigator)\n5. CTA evidence of RV\u002FLV ratio \\> 0.9 note: based on Investigator's interpretation of RV\u002FLV ratio at baseline;\n6. Systolic BP ≥ 90 mmHg note: initial SBP may be \\\u003C 90 mmHg but ≥ 80 mmHg if the pressure recovers with volume resuscitation\n7. Stable heart rate (HR) \\\u003C 130 BPM prior to procedure\n8. Patient is deemed medically eligible for interventional procedure(s), per investigator guidelines and clinical judgment.\n9. Subject or legally authorized representative (LAR) is willing and able to provide written informed consent prior to receiving any non-standard of care protocol specific procedures\n\nExclusion Criteria:\n\n1. Prior PE \\\u003C 180 days from index procedure\n2. Thrombolytic use \\\u003C 48 hours prior to baseline CTA\n3. Pulmonary hypertension with peak pulmonary artery systolic pressure (PASP) \\>70 mmHg by right heart catheterization\n4. Vasopressor requirement after fluids to keep pressure at ≥90 mmHg\n5. FiO2 requirement \\>40% or \\>6 LPM to keep oxygen saturation \\>90%\n6. Hematocrit \\\u003C28% (Note: hematocrit required within 6 hrs. of index procedure)\n7. Platelets count \\\u003C100,000\u002FµL\n8. eGFR \\\u003C30 ml\u002Fmin per 1.73 m2\n9. International normalized ratio (INR) \\>3\n10. Major trauma injury severity score (ISS) \\> 15\n11. Presence of intracardiac lead in right ventricle or atrium placed within 6 months prior to screening assessment\n12. Cardiovascular or pulmonary surgery within 7 days of index procedure\n13. Actively progressing cancer treated by chemotherapeutics\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. History of underlying lung disease that is oxygen dependent\n20. History of chest irradiation\n21. History of heparin-induced thrombocytopenia (HIT)\n22. Contraindication to systemic or therapeutic doses of anticoagulants\n23. Known anaphylactic reaction to radiographic contrast agents that cannot be pretreated\n24. Known residual iliac deep vein thrombosis (DVT), inferior vena cava (IVC) clot or clot in transit (right atrium and\u002For right ventricle).\n25. CTA imaging or other evidence that suggest, in the opinion of the investigator, the Subject is not appropriate for aspiration thrombectomy intervention (e.g., inability to navigate to target location, predominantly chronic clot or non-clot embolus)\n26. Life expectancy \\\u003C90 days, as determined by investigator\n27. Female who is pregnant or nursing\n28. Current participation in another investigational drug or device treatment study Note: observational or registry studies may be permitted with Sponsor approval","90 Years",{"count":47,"type":19},15,[22],"This study is a prospective, single-arm, non-randomized, interventional, multicenter feasibility study to evaluate the safety and effectiveness of percutaneous mechanical thrombectomy using the Akura Thrombectomy System in subjects with acute pulmonary embolism (PE).",[25],"2025-07-24",{"date":53,"type":30},"2025-07-28",{"date":55,"type":30},"2025-02-15",{"date":57,"type":19},"2026-02",{"name":36,"class":37},1,{"id":61,"slug":62,"hasResults":11,"nctId":63,"briefTitle":64,"officialTitle":65,"acronym":4,"eligibilityCriteria":66,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":45,"enrollmentInfo":67,"targetDuration":4,"studyType":20,"phases":69,"briefSummary":70,"conditions":71,"keywords":4,"overallStatus":26,"whyStopped":4,"lastUpdateSubmitDate":51,"lastUpdatePostDateStruct":72,"startDateStruct":73,"completionDateStruct":75,"leadSponsor":77,"locationsCount":78},"100527790","safety-and-effectiveness-of-the-atc-system-in-the-treatment-of-acute-pe-100527790","NCT06152341","Safety and Effectiveness of the ATC System in the Treatment of Acute PE","Safety and Effectiveness of the ATC System in the Treatment of Acute Pulmonary Embolism","Inclusion Criteria:\n\n1. Patient is ≥ 18 and ≤ 90 years old\n2. Clinical signs and symptoms consistent with acute PE for \\\u003C 14 days\n3. CTA evidence of proximal PE\n4. RV\u002FLV ratio \\> 0.9\n5. Systolic BP ≥90 mmHg without the need for vasopressors\n6. Stable heart rate (HR) \\\u003C 130 BPM prior to procedure\n7. Patient is deemed medically eligible for interventional procedure(s), per investigator guidelines and clinical judgment\n8. Subject or legally authorized representative (LAR) is willing and able to provide written informed consent prior to receiving any non-standard of care protocol specific procedures\n\nExclusion Criteria:\n\n1. Prior PE \\\u003C 180 days from index procedure\n2. Thrombolytic use \\\u003C 30 days prior to baseline CTA\n3. Pulmonary hypertension with peak pulmonary artery systolic pressure (PASP) \\>70 mmHg by right heart catheterization\n4. FiO2 requirement \\>40% or \\>6 LPM to keep oxygen saturation \\>90%\n5. Hematocrit \\\u003C28%\n6. Platelets count \\\u003C100,000\u002FµL\n7. Serum creatinine \\>1.8 mg\u002FdL\n8. International normalized ratio (INR) \\>3\n9. Major trauma injury severity score (ISS) \\>15 prior to screening assessment\n10. Presence of intracardiac lead in right ventricle or atrium placed within 6 months prior to screening assessment\n11. Cardiovascular or pulmonary surgery within 7 days of index procedure\n12. Actively progressing cancer treated by chemotherapeutics\n13. Known bleeding diathesis or coagulation disorder\n14. Left bundle branch block\n15. History of severe or chronic pulmonary arterial hypertension\n16. History of chronic left heart disease with left ventricular ejection fraction ≤ 30%\n17. History of decompensated heart failure\n18. History of underlying lung disease that is oxygen dependent\n19. History of chest irradiation\n20. History of heparin-induced thrombocytopenia (HIT)\n21. Contraindication to systemic or therapeutic doses of anticoagulants\n22. Known anaphylactic reaction to radiographic contrast agents that cannot be pretreated\n23. Imaging evidence or other evidence that suggest, in the opinion of the investigator, the Subject is not appropriate for aspiration thrombectomy intervention\n24. Life expectancy \\\u003C90 days, as determined by investigator such as stage 4 cancer, frailty or severe COVID infections\n25. Female who is pregnant or nursing\n26. Current participation in another investigational drug or device treatment study.",{"count":68,"type":19},30,[22],"This study is a prospective, single-arm, interventional, multicenter study to evaluate the safety and effectiveness of the ATC System in subjects with acute pulmonary embolism (PE).",[25],{"date":53,"type":30},{"date":74,"type":30},"2024-05-15",{"date":76,"type":19},"2025-09-15",{"name":36,"class":37},4,""]