[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Imperative Care, Inc.\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":80},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,51],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":23,"conditions":24,"keywords":27,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":39,"lastUpdatePostDateStruct":40,"startDateStruct":43,"completionDateStruct":45,"leadSponsor":47,"locationsCount":50},"100630767","continuous-dual-aspiration-technique-with-zoom-system-for-stroke-100630767",false,"NCT07491952","Continuous Dual Aspiration Technique With Zoom System for Stroke","Clinical Evaluation of Continuous Dual Aspiration Technique With Zoom System for Stroke (ADAPT 2.0)","ADAPT 2 0","Inclusion Criteria:\n\n1. Subject is ≥ 18 years of age\n2. Subject or legally authorized representative has provided written informed consent prior to any study-specific procedures and no later than 72 hours after the index procedure\n3. Pre-stroke mRS 0-2\n4. Subject is undergoing or has undergone an aspiration thrombectomy using the Zoom System with Continuous Dual Aspiration Technique (CDAT) as the first line device within its intended use\n\nExclusion Criteria:\n\n1. Subjects with a life expectancy of less than 6 months\n2. Female subject who is known to be pregnant at time of admission\n3. Any intracranial hemorrhage in the qualifying head CT or MRI\n4. Presence of tandem internal carotid artery occlusion, multiple occlusion locations (e.g., cavernous ICA and M1, separate M2 occlusions, etc.), or occlusions in multiple territories (e.g., MCA and ACA, bilateral, etc.).\n5. In the opinion of the Investigator, the patient is not a suitable candidate for intervention with the Zoom System\n6. Subject is currently enrolled in or planned to be enrolled in any concurrent interventional study that may impact the safety or performance data collected in this study","ALL","18 Years",{"count":20,"type":21},750,"ESTIMATED","OBSERVATIONAL","This study is designed to evaluate the effectiveness, safety and clinical performance of ADAPT 2.0, first-line aspiration neurothrombectomy with Zoom System with Continuous Dual Aspiration Technique (CDAT).",[25,26],"Ischemic Stroke","Acute Stroke",[28,29,30,31,32,33,34,35,36,37],"stroke","thrombectomy","Zoom","aspiration","reperfusion","mRS","ADAPT","continuous","dual aspiration","Zoom System","RECRUITING","2026-06-26",{"date":41,"type":42},"2026-06-29","ACTUAL",{"date":44,"type":42},"2026-03-24",{"date":46,"type":21},"2030-06-01",{"name":48,"class":49},"Imperative Care, Inc.","INDUSTRY",16,{"id":52,"slug":53,"hasResults":11,"nctId":54,"briefTitle":55,"officialTitle":56,"acronym":57,"eligibilityCriteria":58,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":59,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":60,"conditions":61,"keywords":65,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":72,"lastUpdatePostDateStruct":73,"startDateStruct":74,"completionDateStruct":76,"leadSponsor":78,"locationsCount":79},"100619890","aspiration-thrombectomy-using-the-symphony-or-prodigy-system-100619890","NCT07350499","Aspiration Thrombectomy Using the Symphony or Prodigy System","Long-Term CLinical Evaluation of Aspiration ThRombectomy Using the Symphony or ProdIgy Thrombectomy System - CLEAR-IT","CLEAR-IT","Inclusion Criteria:\n\n1. Subject is ≥ 18 years of age\n2. Subject is willing and able to comply with the follow-up schedule specified in this protocol\n3. Subject is willing and able to provide written informed consent prior to any study-related data collection\n4. Subject has a planned procedure, involving the use of Imperative Care vascular devices within their intended use\n\nExclusion Criteria:\n\n1. Subjects with any contraindications per the applicable Instructions for Use\n2. Subject with life expectancy of less than 1 year\n3. In the opinion of the Investigator, the patient is not a suitable candidate for intervention with Imperative Care devices\n4. Subject who may be unable to complete study follow-up\n5. Peripheral Venous Cohort ONLY: Presence of thrombus extending more than 2 cm into the IVC on imaging",{"count":20,"type":21},"The study is designed to evaluate the short-term and long-term clinical performance and safety of the Symphony and Prodigy thrombectomy systems used in endovascular procedures across the peripheral or pulmonary vasculature.",[62,63,64],"Arterial Thromboembolism","Venous Thromboembolism","Pulmonary Embolism",[64,66,67,68,69,70,71],"Thrombus","Thromboembolism","Aspiration","Aspiration thrombectomy","Anticoagulation","Peripheral vasculature","2026-06-23",{"date":39,"type":42},{"date":75,"type":42},"2026-02-13",{"date":77,"type":21},"2030-09",{"name":48,"class":49},4,""]