[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100573126":3},{"organization":4,"armGroups":7,"interventions":18,"overallOfficials":24,"centralContacts":25,"locations":35,"responsibleParty":72,"collaborators":24,"id":74,"slug":75,"hasResults":76,"nctId":77,"briefTitle":78,"officialTitle":79,"acronym":80,"eligibilityCriteria":81,"healthyVolunteers":82,"sex":83,"minAge":84,"maxAge":24,"enrollmentInfo":85,"targetDuration":24,"studyType":88,"phases":89,"briefSummary":91,"conditions":92,"keywords":94,"overallStatus":99,"whyStopped":24,"lastUpdateSubmitDate":100,"lastUpdatePostDateStruct":101,"startDateStruct":104,"completionDateStruct":106,"leadSponsor":108,"locationsCount":109},{"fullName":5,"class":6},"Caption Health, Inc.","INDUSTRY",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Group 1: Pregnant Subjects","OTHER","This group is for pregnant subjects. They will have two ultrasound scans performed- One will be the standard of care ultrasound scan and the other will be research scan",[13],"Device: Research Ultrasound scan",{"label":15,"type":10,"description":16,"interventionNames":17},"Group 2- Non pregnant Subjects","This group is for non-pregnant subjects. They will have one ultrasound scan performed- it will be the research scan",[13],[19],{"type":20,"name":21,"description":22,"armGroupLabels":23,"otherNames":24},"DEVICE","Research Ultrasound scan","Both the study groups will be asked to undergo a research scan performed by an FDA approved ultrasound device",[9,15],null,[26,31],{"name":27,"role":28,"phone":29,"phoneExt":24,"email":30},"Reshma Rajan-Joy, PhD","CONTACT","445-221-3076","reshma.rajan-joy@gehealthcare.com",{"name":32,"role":28,"phone":33,"phoneExt":24,"email":34},"Yngvil Thomas","312-316-5632","yngvil.thomas@gehealthcare.com",[36,57],{"facility":37,"status":24,"city":38,"state":39,"zip":40,"country":41,"countryCode":42,"cosmosGeoPoint":43,"geoPoint":48,"contacts":49},"University of Minnesota","Minneapolis","Minnesota","55455","United States","US",{"type":44,"coordinates":45},"Point",[46,47],-93.26384,44.97997,{"lat":47,"lon":46},[50,54],{"name":51,"role":28,"phone":52,"phoneExt":24,"email":53},"Cresta Jones, MD","612-301-3408","jonesc@umn.edu",{"name":55,"role":28,"phone":24,"phoneExt":24,"email":56},"Maria Bunch","mbunch@umn.edu",{"facility":58,"status":24,"city":59,"state":60,"zip":61,"country":41,"countryCode":42,"cosmosGeoPoint":62,"geoPoint":66,"contacts":67},"Baylor College of Medicine","Houston","Texas","77030",{"type":44,"coordinates":63},[64,65],-95.36327,29.76328,{"lat":65,"lon":64},[68],{"name":69,"role":28,"phone":70,"phoneExt":24,"email":71},"Joan Mastrobattista, MD","281-491-6830","mastroba@bcm.edu",{"type":73,"investigatorFullName":24,"investigatorTitle":24,"investigatorAffiliation":24,"oldNameTitle":24,"oldOrganization":24},"SPONSOR","100573126","clinical-data-collection-for-obstetric-ultrasound-algorithms-100573126",false,"NCT06742229","Clinical Data Collection for Obstetric Ultrasound Algorithms","Prospective Clinical Data Collection for Developing Machine Learning-assisted Obstetric Ultrasound (MOBUS) Screening Algorithms","MOBUS","Inclusion Criteria:\n\nPregnant group (Group 1)\n\n1. Participants aged 18 years or older at time of consent.\n2. Participants with confirmed pregnancy (positive HCG urine test strip and\u002For a documented obstetric ultrasound scan.\n3. Participants who are scheduled for or referred for a standard-of-care clinical obstetric ultrasound examination.\n4. Participants who provide written consent.\n\nNon-pregnant group (Group 2)\n\n1. Participants aged 18 years or older at time of consent.\n2. Participants who are not actively pregnant (confirmed using an HCG urine test strip).\n3. Participants who provide written informed consent.\n\nExclusion Criteria:\n\n\\- 1. Participants for whom participating in this study would delay or compromise care in any way.\n\n2\\. Participants who are not able to understand or provide written consent.",true,"FEMALE","18 Years",{"count":86,"type":87},700,"ESTIMATED","INTERVENTIONAL",[90],"NA","The goal of this clinical trial is to\n\n* Collect ultrasound data from pregnant and non-pregnant individuals presenting to multiple study sites.\n* Use the collected data and ultrasound images to train and validate Artificial intelligence algorithms developed by the Sponsor\n\nConsented participants will be asked to take part in a research ultrasound scan",[93],"Pregnancy",[95,96,97,98],"Obstetrics","Gynecology","Artificial Intelligence","Machine Learning","NOT_YET_RECRUITING","2024-12-17",{"date":102,"type":103},"2024-12-19","ACTUAL",{"date":105,"type":87},"2024-12-20",{"date":107,"type":87},"2025-12-30",{"name":5,"class":6},2]