[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100461885":3},{"organization":4,"armGroups":7,"interventions":26,"overallOfficials":32,"centralContacts":36,"locations":42,"responsibleParty":59,"collaborators":61,"id":65,"slug":66,"hasResults":67,"nctId":68,"briefTitle":69,"officialTitle":69,"acronym":10,"eligibilityCriteria":70,"healthyVolunteers":71,"sex":72,"minAge":73,"maxAge":10,"enrollmentInfo":74,"targetDuration":10,"studyType":77,"phases":10,"briefSummary":78,"conditions":79,"keywords":10,"overallStatus":45,"whyStopped":10,"lastUpdateSubmitDate":83,"lastUpdatePostDateStruct":84,"startDateStruct":87,"completionDateStruct":89,"leadSponsor":91,"locationsCount":92},{"fullName":5,"class":6},"University of Wisconsin, Madison","OTHER",[8,14,18,22],{"label":9,"type":10,"description":11,"interventionNames":12},"Healthy participants",null,"70 healthy participants will be recruited, across substudies 1, 2, 4, and 5",[13],"Device: Non-contrast MRI with novel MRI software",{"label":15,"type":10,"description":16,"interventionNames":17},"Participants with known or suspected iron overload","30 Participants with known or suspected iron overload will be recruited, to substudy 3",[13],{"label":19,"type":10,"description":20,"interventionNames":21},"Participants with elevated levels of liver fat","30 participants with elevated levels of liver fat will be recruited, to substudy 3",[13],{"label":23,"type":10,"description":24,"interventionNames":25},"Participants referred for clinical abdominal MRI","60 participants referred for clinical abdominal MRI will be recruited, to substudy 6",[13],[27],{"type":28,"name":29,"description":30,"armGroupLabels":31,"otherNames":10},"DEVICE","Non-contrast MRI with novel MRI software","The investigational software being used in automatic prescription of the imaging is an application of an AI algorithm. This software prescribes where the MRI system will take images by finding the liver within a set of localizer scans. The software gives coordinates to the scanner.",[9,23,19,15],[33],{"name":34,"affiliation":5,"role":35},"Scott Reeder, MD, PhD","PRINCIPAL_INVESTIGATOR",[37],{"name":38,"role":39,"phone":40,"phoneExt":10,"email":41},"Radiology Studies","CONTACT","608-282-8349","radstudy@uwhealth.org",[43],{"facility":44,"status":45,"city":46,"state":47,"zip":48,"country":49,"countryCode":50,"cosmosGeoPoint":51,"geoPoint":56,"contacts":57},"University of Wisconsin","RECRUITING","Madison","Wisconsin","53705","United States","US",{"type":52,"coordinates":53},"Point",[54,55],-89.40123,43.07305,{"lat":55,"lon":54},[58],{"name":34,"role":35,"phone":10,"phoneExt":10,"email":10},{"type":60,"investigatorFullName":10,"investigatorTitle":10,"investigatorAffiliation":10,"oldNameTitle":10,"oldOrganization":10},"SPONSOR",[62],{"name":63,"class":64},"National Institute for Biomedical Imaging and Bioengineering (NIBIB)","NIH","100461885","fully-automated-high-throughput-quantitative-mri-of-the-liver-100461885",false,"NCT05294471","Fully Automated High-Throughput Quantitative MRI of the Liver","Eligibility Criteria for Substudies 1, 2, 4, 5\n\nInclusion Criteria:\n\n* Age 18 years or older\n\nExclusion Criteria:\n\n* Patients with contraindication to MRI (e.g. pacemaker, contraindicated metallic implants, claustrophobia, etc)\n* Pregnant or trying to become pregnant (as determined by self-report during MRI safety screening)\n\nEligibility Criteria for Substudy 3\n\nInclusion Criteria:\n\n* Age 7 years or older\n* One of:\n\n  * Known or suspected liver iron overload\n  * Known or suspected elevated liver fat\n\nExclusion Criteria:\n\n* Patients with contraindication to MRI (e.g. pacemaker, contraindicated metallic implants, claustrophobia, etc)\n* Patients requiring intravenous (IV) conscious sedation for imaging are not eligible; patients requiring mild, oral anxiolytics for the MRI will be allowed to participate as long as the following criteria are met:\n\n  * The subject has their own prescription for the medication.\n  * The informed consent process is conducted prior to the self-administration of this medication\n  * They come to the research visit with a driver\n* Pregnant or trying to become pregnant (as determined by self-report during MRI safety screening)\n\nEligibility Criteria for Substudy 6\n\nInclusion Criteria:\n\n* Age 7 years or older\n* Scheduled for a clinical abdominal MRI exam\n\nExclusion Criteria:\n\n* Patients with contraindication to MRI (e.g. pacemaker, contraindicated metallic implants, claustrophobia, etc)\n* Sedation required for MRI\n* Pregnant or trying to become pregnant (as determined by self-report during MRI safety screening)",true,"ALL","7 Years",{"count":75,"type":76},200,"ESTIMATED","OBSERVATIONAL","The purpose of this research is to see if a new automated magnetic resonance imaging (MRI) method will be able to improve the images taken of the liver. Participants will have either known or suspected liver disease, known or suspected iron overload syndrome, or be a healthy adult. Participants will be in the research study for one day.",[80,81,82],"Healthy","Iron Overload","Liver Fat","2026-03-09",{"date":85,"type":86},"2026-03-12","ACTUAL",{"date":88,"type":86},"2023-10-16",{"date":90,"type":76},"2026-09",{"name":5,"class":6},1]