[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"SB Technology, Inc.\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":69},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,44],{"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":29,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":32,"lastUpdatePostDateStruct":33,"startDateStruct":36,"completionDateStruct":38,"leadSponsor":40,"locationsCount":43},"100656173","discovery2-study-of-using-mcg-at-emergency-departments-100656173",false,"NCT07822581","\"Discovery2\" Study of Using MCG at Emergency Departments","\"Discovery2\" Study of Using Magnetocardiography (MCG) at Emergency Departments","Discovery2","Inclusion Criteria:\n\n* Women and men aged 22 years and older\n* Participant presenting with signs and symptoms suggestive of NSTE-ACS\n* In ED chest pain\u002FNSTE-ACS care pathway\n* HEART Score 4+\n* Have received their first troponin result and can accommodate an MCG scan before the second troponin result.\n\nExclusion Criteria:\n\n* Unable to provide informed consent\n* ST elevation myocardial infarction (STEMI)\n* Active arrhythmia (as seen on the most recent ECG) such as atrial fibrillation, atrial flutter, ventricular tachycardia\n* Acute hemodynamic instability\n* Inability to lie supine and still for 5-10 minutes\n* Known or suspected pregnancy\n* Unable or unwilling to comply with required follow-up\n* Metallic passive implants that would make the participant unsuitable for MCG (e.g. spinal implants, metal shoulder replacements, dental implants.. etc.)\n* Active implantable medical devices (e.g. pacemakers, neurostimulators.. etc.)\n* Active illegal drug use per history of present illness\n* Contraindicated for temporary removal of telemetry during MCG scan\n* Clear non-ischemic cause for symptoms (e.g. trauma, viral infection, valve disease)\n* Clinical conditions that in the opinion of the Investigator would compromise the safety of the participant or ability to complete the protocol (e.g., exceeds bed weight limit, allergy to adhesives)","ALL","22 Years",{"count":20,"type":21},200,"ESTIMATED","OBSERVATIONAL","The purpose of this research is to collect the magnetic signals from the heart to identify features that may help Emergency Department (ED) doctors differentiate high and low risk patients for heart related chest pain.",[25,26,27,28],"Acute Coronary Syndromes (ACS)","Coronary Artery Disease (CAD)","Chest Pain","NSTE-ACS (NSTEMI and UA)",[30],"Magnetocardiography (MCG)","NOT_YET_RECRUITING","2026-09-11",{"date":34,"type":35},"2026-09-16","ACTUAL",{"date":37,"type":21},"2026-09-01",{"date":39,"type":21},"2027-03-30",{"name":41,"class":42},"SB Technology, Inc.","INDUSTRY",1,{"id":45,"slug":46,"hasResults":11,"nctId":47,"briefTitle":48,"officialTitle":49,"acronym":50,"eligibilityCriteria":51,"healthyVolunteers":11,"sex":17,"minAge":52,"maxAge":4,"enrollmentInfo":53,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":55,"conditions":56,"keywords":58,"overallStatus":61,"whyStopped":4,"lastUpdateSubmitDate":37,"lastUpdatePostDateStruct":62,"startDateStruct":64,"completionDateStruct":66,"leadSponsor":68,"locationsCount":5},"100553119","a-prospective-research-investigation-of-ischemia-using-mcg-100553119","NCT06481943","A Prospective Research Investigation of Ischemia Using MCG","A Prospective Research Investigation of Ischemia Using SandboxAQ Magnetocardiography Device","PRISM\u002FPRISM2","Inclusion Criteria:\n\n* Scheduled to undergo a diagnostic angiography or revascularization procedure for the diagnosis or treatment of ischemia or acute myocardial infarction\n* Ability for participant to comply with study requirements\n* Patient consented before the planned, clinically indicated cath-lab procedure begins to allow sufficient time for study related activities\n* Written informed consent\n\nExclusion Criteria:\n\n* Present STEMI\n* Pregnant or breastfeeding\n* Having an active atrial fibrillation episode as seen on most current 12-lead ECG\n* Active thoracic metal implant\n* Poor access to follow-up","18 Years",{"count":54,"type":21},335,"PRISM is a prospective, pilot research study that aims to systematically characterize the usefulness of CardiAQ MCG, a bedside magnetocardiography device, in the evaluation of myocardial ischemia and infarction status.",[57],"Acute Coronary Syndrome",[59,60],"Magnetocardiography","MCG","RECRUITING",{"date":63,"type":35},"2026-09-04",{"date":65,"type":35},"2024-07-11",{"date":67,"type":21},"2027-02",{"name":41,"class":42},""]