[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100537945":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":21,"centralContacts":25,"locations":31,"responsibleParty":53,"collaborators":20,"id":55,"slug":20,"hasResults":56,"nctId":57,"briefTitle":58,"officialTitle":59,"acronym":20,"eligibilityCriteria":60,"healthyVolunteers":61,"sex":62,"minAge":63,"maxAge":64,"enrollmentInfo":65,"targetDuration":20,"studyType":68,"phases":69,"briefSummary":71,"conditions":72,"keywords":20,"overallStatus":33,"whyStopped":20,"lastUpdateSubmitDate":75,"lastUpdatePostDateStruct":76,"startDateStruct":79,"completionDateStruct":81,"leadSponsor":83,"locationsCount":84},{"fullName":5,"class":6},"University of Chicago","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"Durometer","EXPERIMENTAL","This is a single-arm trial in which a Shore durometer will be used to measure the hardness of the uterus after placental delivery during cesarean section.",[13],"Device: Shore durometer",[15],{"type":16,"name":17,"description":18,"armGroupLabels":19,"otherNames":20},"DEVICE","Shore durometer","The durometer will be held on the exterior of the lower uterine segment and fundus to measure the hardness reading at each location.",[9],null,[22],{"name":23,"affiliation":5,"role":24},"Naida Cole, MD","PRINCIPAL_INVESTIGATOR",[26],{"name":27,"role":28,"phone":29,"phoneExt":20,"email":30},"Al McAuley","CONTACT","(773) 834-3274","amcauley1@dacc.uchicago.edu",[32],{"facility":5,"status":33,"city":34,"state":35,"zip":36,"country":37,"cosmosGeoPoint":38,"geoPoint":43,"contacts":44},"RECRUITING","Chicago","Illinois","60637","United States",{"type":39,"coordinates":40},"Point",[41,42],-87.65005,41.85003,{"lat":42,"lon":41},[45,49],{"name":46,"role":28,"phone":47,"phoneExt":20,"email":48},"Naida M Cole, MD","773-702-6700","nmcole@bsd.uchicago.edu",{"name":50,"role":28,"phone":51,"phoneExt":20,"email":52},"Somayeh Mohammadi","17738343274","mohammadis@bsd.uchicago.edu",{"type":54,"investigatorFullName":20,"investigatorTitle":20,"investigatorAffiliation":20,"oldNameTitle":20,"oldOrganization":20},"SPONSOR","100537945",false,"NCT06284421","Durometer for Measuring Uterine Tone","Use of a Durometer to Measure Uterine Tone in Cesarean Delivery","Inclusion Criteria:\n\n* Non-emergent (scheduled) cesarean delivery at University of Chicago Family Birth Center\n* Patients ages 18-50\n\nExclusion Criteria:\n\n* Patients undergoing unscheduled (intrapartum) cesarean delivery\n* Ages \\\u003C18 or \\>50 years old\n* Intrapartum cesarean hysterectomy\n* Inability to provide independent, informed consent due to impairment or intellectual disability\n* Non-English speaking patients",true,"FEMALE","18 Years","50 Years",{"count":66,"type":67},20,"ESTIMATED","INTERVENTIONAL",[70],"NA","This study will evaluate the use of a durometer to measure uterine tone in parturients undergoing cesarean delivery.",[73,74],"Uterine Tone Disorders","Cesarean Section Complications","2025-05-05",{"date":77,"type":78},"2025-05-06","ACTUAL",{"date":80,"type":78},"2024-02-08",{"date":82,"type":67},"2026-08-30",{"name":5,"class":6},1]