[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Heartstream US LLC\",\"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,[8,41,55],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":11,"sex":15,"minAge":4,"maxAge":4,"enrollmentInfo":16,"targetDuration":19,"studyType":20,"phases":4,"briefSummary":21,"conditions":22,"keywords":24,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":29,"lastUpdatePostDateStruct":30,"startDateStruct":33,"completionDateStruct":35,"leadSponsor":37,"locationsCount":40},"100427037","heartstart-hs1-defibrillator-event-registry-100427037",false,"NCT04840797","HeartStart HS1 Defibrillator* Event Registry","Inclusion Criteria:\n\n* Have been suspected of a circulatory arrest for any cause.\n* Have had HeartStart HS1 Defibrillator with electrodes:\n\nAdult SMART Pads Cartridge \\[REF: M5071A\\], Infant\u002FChild SMART Pads Cartridge (REF:M5072A) applied to their body and powered up with HS1 battery (Model M5070A), regardless of whether a defibrillation shock was delivered\n\nExclusion Criteria:\n\n* Subjects will be excluded if any of the following are present:\n* AED or pad use other than the HeartStart HS1 Defibrillator with above referenced Philips electrode pads. Note: Use of a device other than the Philips HeartStart HS1 AED does not preclude enrollment if the AED or an Advanced Life Support defibrillator was used after the HeartStart HS1 AED.\n* AED used for training purposes.","ALL",{"count":17,"type":18},1400,"ESTIMATED","1 Day","OBSERVATIONAL","A Prospective study on the performance and safety of the HeartStart OnSite (Model M5066A) \\& HeartStart Home (Model M5068A) Defibrillator device data.",[23],"Sudden Cardiac Arrest",[25,26,27],"AED","Post -Market","Cardiology","RECRUITING","2026-08-07",{"date":31,"type":32},"2026-08-11","ACTUAL",{"date":34,"type":32},"2021-02-25",{"date":36,"type":18},"2030-12-31",{"name":38,"class":39},"Heartstream US LLC","INDUSTRY",1,{"id":42,"slug":43,"hasResults":11,"nctId":44,"briefTitle":45,"officialTitle":45,"acronym":4,"eligibilityCriteria":46,"healthyVolunteers":11,"sex":15,"minAge":4,"maxAge":4,"enrollmentInfo":47,"targetDuration":19,"studyType":20,"phases":4,"briefSummary":48,"conditions":49,"keywords":4,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":29,"lastUpdatePostDateStruct":50,"startDateStruct":51,"completionDateStruct":53,"leadSponsor":54,"locationsCount":40},"100381764","heartstart-frx-defibrillator-event-registry-100381764","NCT04250857","HeartStart FRx Defibrillator Event Registry","Inclusion Criteria:\n\n* Subjects accepted into the study must: have been suspected of a circulatory arrest for any cause\n* Have had HeartStart FRx AED with electrodes: HeartStart SMART PADS II applied to their body and powered up, regardless of whether a defibrillation shock was delivered\n\nExclusion Criteria:\n\n* AED or pad use other than the HeartStart FRx AED with electrodes : HeartStart SMART PADS II\n* AED used for training purposes.",{"count":17,"type":18},"This post market clinical follow-up study is a multi-center, non-randomized, unblinded, observational registry of the performance of the FRx Automated external defibrillator (AED) used in conjunction with electrodes with or without use of the infant\u002Fchild key. The registry is focused only on on post-event data collection and does not prescribe any device usage. This registry has several safeguards in place to prevent against selections bias, including enrollment of all participants who have pads placed. This registry will evaluate the safety and verify the clinical performance of the device in relation to its claims, when used in accordance with the Device Manual.",[23],{"date":31,"type":32},{"date":52,"type":32},"2019-11-04",{"date":36,"type":18},{"name":38,"class":39},{"id":56,"slug":57,"hasResults":11,"nctId":58,"briefTitle":59,"officialTitle":59,"acronym":4,"eligibilityCriteria":60,"healthyVolunteers":11,"sex":15,"minAge":61,"maxAge":62,"enrollmentInfo":63,"targetDuration":4,"studyType":20,"phases":4,"briefSummary":65,"conditions":66,"keywords":4,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":71,"lastUpdatePostDateStruct":72,"startDateStruct":74,"completionDateStruct":76,"leadSponsor":78,"locationsCount":40},"100649042","pulse-detection-in-cardiac-arrest-patients-using-a-doppler-ultrasound-patch-on-the-carotid-artery-100649042","NCT07729228","Pulse Detection in Cardiac Arrest Patients Using a Doppler Ultrasound Patch on the Carotid Artery","Inclusion Criteria:\n\n* Any adult patient aged \\> 18 to 99 years old\n* Intact skin on their neck\n* In cardiac arrest with an arterial line placed during the resuscitation event as part of the standard of care.\n\nExclusion Criteria:\n\n* Patients in cardiac arrest with a Do Not Resuscitate\u002FDo Not Intubate (DNR\u002FDNI) order.\n* Patients without an arterial line in place as part of the standard of care.\n* \\*Pregnant women\n* \\*Prisoners\n\n  * Any data from these two populations (pregnant\u002Fprisoner) will not be downloaded at all if it is discovered post-resuscitation event that the patient is pregnant and\u002For a prisoner.","18 Years","99 Years",{"count":64,"type":18},20,"The purpose of this study is to find out if a Doppler ultrasound patch placed on the neck can accurately and quickly detect when a cardiac arrest patient's heart starts beating again (return of spontaneous circulation, or ROSC) during resuscitation in the emergency department. The study compares the ultrasound readings to data from an arterial line, which is considered the most reliable way to check for a pulse. The main question the study is trying to answer is whether using Doppler ultrasound is better than the traditional method of feeling for a pulse, which can be unreliable, especially in stressful situations. Secondarily, this study aims to assess blood flow through the carotid artery from chest compressions during resuscitative events to determine overall effectiveness. This research hopes to show that Doppler ultrasound can help medical teams recognize when a patient's heart has restarted more accurately and quickly, leading to better care during cardiac arrest.",[67,68,69],"Cardiac Arrest (CA)","Return of Spontaneous Circulation","CPR Quality Assessment","NOT_YET_RECRUITING","2026-07-24",{"date":73,"type":32},"2026-07-27",{"date":75,"type":18},"2026-08-15",{"date":77,"type":18},"2027-08-15",{"name":38,"class":39},""]