[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100611896":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":20,"centralContacts":24,"locations":19,"responsibleParty":33,"collaborators":35,"id":39,"slug":40,"hasResults":41,"nctId":42,"briefTitle":43,"officialTitle":44,"acronym":19,"eligibilityCriteria":45,"healthyVolunteers":46,"sex":47,"minAge":48,"maxAge":19,"enrollmentInfo":49,"targetDuration":19,"studyType":52,"phases":53,"briefSummary":55,"conditions":56,"keywords":58,"overallStatus":60,"whyStopped":19,"lastUpdateSubmitDate":61,"lastUpdatePostDateStruct":62,"startDateStruct":65,"completionDateStruct":67,"leadSponsor":69,"locationsCount":19},{"fullName":5,"class":6},"University of Utah","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"CPAP","EXPERIMENTAL","Airway pressure support through the investigational device",[13],"Device: CPAP",[15],{"type":16,"name":9,"description":17,"armGroupLabels":18,"otherNames":19},"DEVICE","Airway pressure support through the investigational device.",[9],null,[21],{"name":22,"affiliation":5,"role":23},"Kai Kuck, PhD","PRINCIPAL_INVESTIGATOR",[25,29],{"name":22,"role":26,"phone":27,"phoneExt":19,"email":28},"CONTACT","(801) 581-6393","kai.kuck@hsc.utah.edu",{"name":30,"role":26,"phone":31,"phoneExt":19,"email":32},"Trey Blackwell, MS","(801) 395-4038","Trey.Blackwell@utah.edu",{"type":34,"investigatorFullName":19,"investigatorTitle":19,"investigatorAffiliation":19,"oldNameTitle":19,"oldOrganization":19},"SPONSOR",[36],{"name":37,"class":38},"Dynasthetics LLC","UNKNOWN","100611896","positive-airway-pressure-pap-system-evaluation-in-volunteers-100611896",false,"NCT07246538","Positive Airway Pressure (PAP) System Evaluation in Volunteers","Evaluation of a Novel Positive Airway Pressure System in Volunteers","Inclusion Criteria:\n\n* Healthy volunteers\n\nExclusion Criteria:\n\n* Have any respiratory or cardiovascular conditions\n* i.e., cold, allergies, congestion, pneumonia, lung cancer, COPD, acute respiratory distress syndrome, etc.",true,"ALL","18 Years",{"count":50,"type":51},25,"ESTIMATED","INTERVENTIONAL",[54],"NA","This study will test the control and measurements of a new system for airway support in healthy volunteers. The goals of the study are to evaluate how accurately the system can stabilize airway pressure to a desired level, evaluate the accuracy of the system's reported volume of each breath (tidal volume), evaluate the accuracy of the system's reported respiratory rate, evaluate the accuracy of exhaled carbon dioxide monitoring with a standard carbon dioxide monitor when the novel PAP system is used, and evaluate general comfort of the volunteers while using the system.",[57],"Obstruction Airway",[59],"Device feasibility","NOT_YET_RECRUITING","2025-12-16",{"date":63,"type":64},"2025-12-23","ACTUAL",{"date":66,"type":51},"2026-02-01",{"date":68,"type":51},"2026-06-30",{"name":5,"class":6}]