[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100543773":3},{"organization":4,"outcomesModule":7,"designInfo":13,"detailedDescription":11,"studyPopulation":16,"armGroups":11,"interventions":17,"overallOfficials":11,"centralContacts":22,"locations":11,"responsibleParty":28,"collaborators":11,"id":30,"slug":11,"hasResults":31,"nctId":32,"briefTitle":33,"officialTitle":33,"acronym":34,"eligibilityCriteria":35,"healthyVolunteers":31,"sex":36,"minAge":37,"maxAge":11,"enrollmentInfo":38,"targetDuration":11,"studyType":41,"phases":11,"briefSummary":42,"conditions":43,"keywords":11,"overallStatus":45,"whyStopped":11,"lastUpdateSubmitDate":46,"lastUpdatePostDateStruct":47,"startDateStruct":50,"completionDateStruct":52,"leadSponsor":54,"locationsCount":11},{"fullName":5,"class":6},"Medistim ASA","INDUSTRY",{"primaryOutcomes":8,"secondaryOutcomes":11,"otherOutcomes":11},[9],{"measure":10,"description":11,"timeFrame":12},"Wide and high-quality dataset uploaded to CaseCloud from CABG-procedures.",null,"1 day",{"allocation":11,"interventionModel":11,"interventionModelDescription":11,"primaryPurpose":11,"observationalModel":14,"timePerspective":15,"maskingInfo":11},"OTHER","PROSPECTIVE","Patients scheduled for cardiac bypass surgery (CABG) that have signed an informed consent form for this study",[18],{"type":19,"name":20,"description":21,"armGroupLabels":11,"otherNames":11},"DEVICE","MiraQ systems with Transit Time Flow Measurement (TTFM) and High Frequency Ultrasound (HFUS) probes","The objective of this study is to harvest a wide dataset of high quality to allow exploratory analysis and training of machine learning",[23],{"name":24,"role":25,"phone":26,"phoneExt":11,"email":27},"Haakon Grøthe","CONTACT","04790968263","haakon.groethe@medistim.com",{"type":29,"investigatorFullName":11,"investigatorTitle":11,"investigatorAffiliation":11,"oldNameTitle":11,"oldOrganization":11},"SPONSOR","100543773",false,"NCT06360224","Collect Flow and Ultrasound Images of Coronary Bypass Grafts","CASES","Inclusion Criteria:\n\n* Patient older than 18 years\n* Scheduled for CABG\n* Understand the nature of the procedure and willingness to comply with the CIP\n* Provide written informed consent\n\nExclusion Criteria:\n\n* Patient younger than 18 years\n* Any condition that the investigator believes should exclude participation","ALL","18 Years",{"count":39,"type":40},100,"ESTIMATED","OBSERVATIONAL","This is a post-market observational, non-interventional, multicenter clinical investigation with the purpose of harvesting high quality data from regular cardiac bypass surgery (CABG).",[44],"Cardiac Bypass Surgery (CABG)","NOT_YET_RECRUITING","2024-04-06",{"date":48,"type":49},"2024-04-11","ACTUAL",{"date":51,"type":40},"2024-05-15",{"date":53,"type":40},"2029-05-15",{"name":5,"class":6}]