[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100645041":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":10,"centralContacts":19,"locations":10,"responsibleParty":29,"collaborators":10,"id":31,"slug":10,"hasResults":32,"nctId":33,"briefTitle":34,"officialTitle":35,"acronym":10,"eligibilityCriteria":36,"healthyVolunteers":32,"sex":37,"minAge":38,"maxAge":39,"enrollmentInfo":40,"targetDuration":10,"studyType":43,"phases":10,"briefSummary":44,"conditions":45,"keywords":10,"overallStatus":50,"whyStopped":10,"lastUpdateSubmitDate":51,"lastUpdatePostDateStruct":52,"startDateStruct":55,"completionDateStruct":57,"leadSponsor":59,"locationsCount":10},{"fullName":5,"class":6},"Medtronic MiniMed, Inc.","INDUSTRY",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"MiniMed Fit Payload adhesive components",null,"Pediatric participants with insulin-requiring diabetes using the MiniMed Fit Payload adhesive components in different wear locations over a 7-day period.",[13],"Device: MiniMed Fit Payload adhesive components",[15],{"type":16,"name":9,"description":17,"armGroupLabels":18,"otherNames":10},"DEVICE","The MiniMed Fit Payload device used in this study will be made of polycarbonate materials, will not contain any electronic or mechanical components, and is intended to mimic the shape and weight of a future product. Each device will consist of the payload assembly and an adhesive patch, which will be adhered to the payload on one side and the subject's skin on the other.",[9],[20,25],{"name":21,"role":22,"phone":23,"phoneExt":10,"email":24},"McKenna Cherry","CONTACT","763-505-1195","mckenna.cherry@medtronic.com",{"name":26,"role":22,"phone":27,"phoneExt":10,"email":28},"Melissa Vella","416-768-0862","melissa.vella@medtronic.com",{"type":30,"investigatorFullName":10,"investigatorTitle":10,"investigatorAffiliation":10,"oldNameTitle":10,"oldOrganization":10},"SPONSOR","100645041",false,"NCT07675161","MiniMed Fit Payload Wear Pediatric Study","CIP361: MiniMed Fit Payload Wear Pediatric Study","Inclusion Criteria:\n\n* Participants with insulin-requiring diabetes\n* Participants 7-17 years of age\n* Participant and parent\u002Fguardian\u002Flegally authorized representative are able and willing to sign informed consent\u002Fassent\n\nExclusion Criteria:\n\n* Participants who report known skin sensitivity or allergy to polycarbonate or pressure-sensitive adhesives, e.g., medical device adhesives, band-aids, other acrylic-containing adhesives.\n* Participants with any skin condition in the area where device placement (e.g., irritation, rash, infection) could occur, per participant report.\n* Participants who are pregnant (per self-report) at initial screening. If a participant becomes pregnant during the study, the site will follow procedures for study withdrawal.","ALL","7 Years","17 Years",{"count":41,"type":42},100,"ESTIMATED","OBSERVATIONAL","The purpose of this study is to assess MiniMed Fit Payload adhesive components in different wear locations over a 7-day period to support development of the future commercialized patch pump in participants 7-17 years of age.",[46,47,48,49],"Diabetes (DM)","Diabetes (Insulin-requiring, Type 1 or Type 2)","Diabetes in Children","Diabetes in Adolescence","NOT_YET_RECRUITING","2026-06-25",{"date":53,"type":54},"2026-06-30","ACTUAL",{"date":56,"type":42},"2026-07",{"date":58,"type":42},"2026-12",{"name":5,"class":6}]