[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"atrial-appendage-closure-for-atrial-fibrillation\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:atrial-appendage-closure-for-atrial-fibrillation":24},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,45],{"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":20,"studyType":21,"phases":4,"briefSummary":22,"conditions":23,"keywords":30,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":35,"startDateStruct":38,"completionDateStruct":40,"leadSponsor":42,"locationsCount":4},"100635406","hummingbird-ice-study-100635406",false,"NCT07552272","Hummingbird ICE Study","Inclusion Criteria:\n\n* 18 years of age\n* Willing to provide written, dated and signed, informed consent\n* Undergoing percutaneous cardiac intervention procedures in with VeriSight Pro is used\n\nExclusion Criteria:\n\n* Contraindicated for ICE catheter placement or considerations that make placement of VeriSight not technically feasible\n* Known contraindicated conditions include sepsis, major coagulation abnormalities, presence of any intracardiac thrombus, presence of class IV angina or heart failure, deep vein thrombosis, or significant peripheral vascular disease","ALL","18 Years",{"count":18,"type":19},1000,"ESTIMATED","2 Days","OBSERVATIONAL","The goals of this observational study are to collect data and ultrasound images using the Philips VeriSight Pro intracardiac echocardiography (ICE) catheter to assess safety and effectiveness and to support development efforts of the VeriSight Pro imaging platform.",[24,25,26,27,28,29],"ATRIAL APPENDAGE CLOSURE for ATRIAL FIBRILLATION","Atrial Fibrillation (AF)","Valve Disease, Heart","Atrial Septal Defect","Patent Foramen Ovale","Tricuspid Valve Disease",[31,32],"Intracardiac Echocardiography (ICE)","VeriSight","NOT_YET_RECRUITING","2026-05-18",{"date":36,"type":37},"2026-05-22","ACTUAL",{"date":39,"type":19},"2026-07",{"date":41,"type":19},"2031-07",{"name":43,"class":44},"Philips Clinical & Medical Affairs Global","INDUSTRY",{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":50,"acronym":51,"eligibilityCriteria":52,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":53,"targetDuration":4,"studyType":55,"phases":56,"briefSummary":58,"conditions":59,"keywords":4,"overallStatus":63,"whyStopped":4,"lastUpdateSubmitDate":64,"lastUpdatePostDateStruct":65,"startDateStruct":67,"completionDateStruct":69,"leadSponsor":71,"locationsCount":74},"100620690","atrial-fibrillation-trial-of-left-atrial-appendage-closure-using-seralene-hemostatic-suture-100620690","NCT07360899","Atrial Fibrillation TRIal of Left Atrial Appendage Closure Using Seralene Hemostatic Suture","Left Atrial Appendage Closure During Cardiac Surgery in Atrial Fibrillation Patients With Seralene","ATRI-LASH","Inclusion Criteria:\n\nAge 18 years or older\n\nDocumented atrial fibrillation (any type)\n\nCHA₂DS₂-VASc score of 2 or greater, or equivalent stroke risk\n\nScheduled to undergo cardiac surgery (including coronary artery bypass grafting, valve surgery, or other structural cardiac surgery)\n\nAbility to understand the study and provide written informed consent\n\nExclusion Criteria:\n\nContraindication to left atrial appendage closure (e.g., presence of left atrial appendage thrombus or unsuitable anatomy)\n\nLife expectancy less than 3 months, based on clinical judgment\n\nCurrent participation in another clinical study that could interfere with the outcomes of this study\n\nActive or suspected infective endocarditis",{"count":54,"type":19},200,"INTERVENTIONAL",[57],"NA","Atrial fibrillation is a common heart rhythm disorder that increases the risk of stroke. In patients with atrial fibrillation, blood clots most often form in a small structure of the heart called the left atrial appendage. If a blood clot travels from the heart to the brain, it can cause a stroke.\n\nBlood-thinning medications are commonly prescribed to reduce the risk of stroke in patients with atrial fibrillation. However, some patients cannot take these medications long-term because of bleeding risk, side effects, or other medical reasons.\n\nClosing the left atrial appendage is an alternative approach to reduce the risk of stroke by preventing blood from collecting in this area. When patients undergo cardiac surgery for another indication, closure of the left atrial appendage can be performed during the same operation.\n\nThis study is designed to evaluate the safety and effectiveness of surgical closure of the left atrial appendage using a device called AtriLASH during cardiac surgery. AtriLASH is a surgical suture-based device intended to close the left atrial appendage.\n\nThe study will assess whether the left atrial appendage can be safely and effectively closed using this method in patients with atrial fibrillation undergoing cardiac surgery. The information obtained from this study may help determine whether this approach can reduce the risk of stroke and potentially decrease the need for long-term use of blood-thinning medications in selected patients.",[24,25,60,61,62],"Mitral Valve Surgery","Stroke (in Patients With Atrial Fibrillation)","Anticoagulant Therapy","RECRUITING","2026-01-14",{"date":66,"type":37},"2026-01-22",{"date":68,"type":37},"2025-12-01",{"date":70,"type":19},"2026-06-30",{"name":72,"class":73},"Institute of Cardiovascular Diseases, Vojvodina","OTHER",1]