[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"coronary-computed-tomographic-angiography\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:coronary-computed-tomographic-angiography":24},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,1,0,[8],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":4,"briefSummary":22,"conditions":23,"keywords":4,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":28,"lastUpdatePostDateStruct":29,"startDateStruct":32,"completionDateStruct":34,"leadSponsor":36,"locationsCount":5},"100570105","gsi-cardiac-on-revolution-apex---us-100570105",false,"NCT06702917","GSI Cardiac on Revolution Apex - US","Wide Coverage GSI Cardiac Data Collection","Inclusion Criteria:\n\nSubjects may be included in this study if they meet the following criteria:\n\n1. Who are ≥18 years of age;\n2. Able to sign and date the informed consent form; AND,\n3. Cohort A: Undergoing a scheduled clinically indicated CCTA; OR,\n4. Cohort B: Known history of myocardial infarction or undergoing a clinically indicated cardiac catheterization due to known pathology.\n\nExclusion Criteria:\n\nSubjects may be excluded from participating in study if they meet any of the following criteria:\n\n1. Who are pregnant or lactating;\n2. Who were previously enrolled in this study;\n3. Anyone with known or suspected allergy to iodinated contrast agents;\n4. Anyone with known or suspected renal insufficiency as determined by site medical personnel;\n5. Who are in need of urgent or emergent care;\n6. Who have any conditions that, in the opinion of the PI or designee, would interfere with the evaluation of the results or constitute a health hazard for the subject;\n7. Who are unwilling to have GEHC personnel present for the CT exam; AND,\n8. Cohort A: Undergoing a scheduled clinically indicated CCTA for anatomy assessment (aberrant origin, etc.)","ALL","18 Years",{"count":19,"type":20},50,"ESTIMATED","OBSERVATIONAL","The goal of this clinical data collection study is to collect raw CT scan data using a new GSI Cardiac mode on GE HealthCare's Revolution Apex CT system.\n\nTwo groups of participants will be enrolled:\n\nA) Participants scheduled to undergo a Coronary CT Angiography (CCTA) as part of their standard of care\n\nB) Participants scheduled to undergo a cardiac catheterization or have a history of heart attack\n\nParticipants in Group A will:\n\n-Have a standard of care CCTA immediately followed by a research GSI Cardiac scan\n\nParticipants in Group B will:\n\n-Have a research CCTA immediately followed by a research GSI Cardiac scan\n\nBoth groups will be in the study for approximately 1 day. There are no follow-up visits after the day of scan.",[24,25,26],"Coronary Computed Tomographic Angiography","Myocardial Infarction (MI)","Cardiac Catheterization","RECRUITING","2026-04-24",{"date":30,"type":31},"2026-04-27","ACTUAL",{"date":33,"type":31},"2025-09-10",{"date":35,"type":20},"2026-06",{"name":37,"class":38},"GE Healthcare","INDUSTRY"]