[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100619445":3},{"organization":4,"armGroups":7,"interventions":7,"overallOfficials":8,"centralContacts":12,"locations":18,"responsibleParty":37,"collaborators":7,"id":40,"slug":41,"hasResults":42,"nctId":43,"briefTitle":44,"officialTitle":45,"acronym":7,"eligibilityCriteria":46,"healthyVolunteers":47,"sex":48,"minAge":49,"maxAge":50,"enrollmentInfo":51,"targetDuration":7,"studyType":54,"phases":7,"briefSummary":55,"conditions":56,"keywords":7,"overallStatus":21,"whyStopped":7,"lastUpdateSubmitDate":65,"lastUpdatePostDateStruct":66,"startDateStruct":69,"completionDateStruct":71,"leadSponsor":73,"locationsCount":74},{"fullName":5,"class":6},"Mayo Clinic","OTHER",null,[9],{"name":10,"affiliation":5,"role":11},"William A. Carey, MD","PRINCIPAL_INVESTIGATOR",[13],{"name":14,"role":15,"phone":16,"phoneExt":7,"email":17},"Lavonne M. Liedl, LRT","CONTACT","507-255-1828","liedl.lavonne@mayo.edu",[19],{"facility":20,"status":21,"city":22,"state":23,"zip":24,"country":25,"countryCode":26,"cosmosGeoPoint":27,"geoPoint":32,"contacts":33},"Mayo Clinic in Rochester","RECRUITING","Rochester","Minnesota","55905","United States","US",{"type":28,"coordinates":29},"Point",[30,31],-92.4699,44.02163,{"lat":31,"lon":30},[34,36],{"name":35,"role":15,"phone":16,"phoneExt":7,"email":17},"Lavonne Liedl, LRT",{"name":10,"role":11,"phone":7,"phoneExt":7,"email":7},{"type":11,"investigatorFullName":38,"investigatorTitle":39,"investigatorAffiliation":5,"oldNameTitle":7,"oldOrganization":7},"William A. Carey","Principal Investigator","100619445","predicting-the-need-for-prolonged-respiratory-support-in-neonates-delivered-in-a-lower-level-nicu-setting-100619445",false,"NCT07344714","Predicting the Need for Prolonged Respiratory Support in Neonates Delivered in a Lower-Level NICU Setting","Predicting Respiratory Distress Syndrome in Neonates Delivered in a Lower-Level NICU Setting","Inclusion Criteria:\n\nBoth of the following:\n\n* Neonates born at 32 completed weeks gestational age or older whose deliveries are attended by the neonatal resuscitation team and for whom routine gastric suctioning is indicated\n* Neonates whose parents actively accepted or did not actively decline the Minnesota Research Authorization.\n\nExclusion Criteria:\n\nAny one of the following:\n\n* Neonates with known or suspected congenital anomalies\n* Neonates for whom only comfort measures are planned or possible at time of delivery\n* Neonates whose parents actively declined the Minnesota Research Authorization.\n* Neonates with other identifiable causes of respiratory distress including pneumothorax, meconium aspiration syndrome, or pneumonia.",true,"ALL","32 Weeks","41 Weeks",{"count":52,"type":53},500,"ESTIMATED","OBSERVATIONAL","The purpose of this study is to analyze the gastric fluid aspirated from the stomachs of neonates receiving routine post-delivery care to predict the need for prolonged respiratory support (\\>6 hours of life).",[57,58,59,60,61,62,63,64],"Respiratory Distress Syndrome, Newborn","Respiratory Distress Syndrome in Premature Infant","Transient Tachypnea of the Newborn","Meconium Aspiration Syndrome","Pneumonia Neonatal","Hyaline Membrane Disease","Pneumothorax","Respiratory Distress Neonatal","2026-03-16",{"date":67,"type":68},"2026-03-18","ACTUAL",{"date":70,"type":68},"2026-03-11",{"date":72,"type":53},"2026-12-31",{"name":5,"class":6},1]