[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100650169":3},{"organization":4,"armGroups":7,"interventions":27,"overallOfficials":10,"centralContacts":41,"locations":50,"responsibleParty":64,"collaborators":66,"id":69,"slug":70,"hasResults":71,"nctId":72,"briefTitle":73,"officialTitle":74,"acronym":10,"eligibilityCriteria":75,"healthyVolunteers":71,"sex":76,"minAge":77,"maxAge":10,"enrollmentInfo":78,"targetDuration":10,"studyType":81,"phases":10,"briefSummary":82,"conditions":83,"keywords":10,"overallStatus":86,"whyStopped":10,"lastUpdateSubmitDate":87,"lastUpdatePostDateStruct":88,"startDateStruct":91,"completionDateStruct":93,"leadSponsor":95,"locationsCount":96},{"fullName":5,"class":6},"C. R. Bard","INDUSTRY",[8,14,18,23],{"label":9,"type":10,"description":11,"interventionNames":12},"Male Indwelling Catheter",null,"Adult male ICU patients with an indwelling urinary catheter for urine output monitoring",[13],"Device: Indwelling Urinary Catheter",{"label":15,"type":10,"description":16,"interventionNames":17},"Female Indwelling Catheter","Adult female ICU patients with an indwelling urinary catheter for urine output monitoring",[13],{"label":19,"type":10,"description":20,"interventionNames":21},"Male External Catheter","Adult male ICU patients with an external urinary catheter for urine output monitoring",[22],"Device: External Urinary Catheter",{"label":24,"type":10,"description":25,"interventionNames":26},"Female External Catheter","Adult female ICU patients with an external urinary catheter for urine output monitoring",[22],[28,35],{"type":29,"name":30,"description":31,"armGroupLabels":32,"otherNames":33},"DEVICE","Indwelling Urinary Catheter","A thin, flexible, sterile tube that is inserted through the urethra into the bladder to drain urine, typically into a urine meter",[15,9],[34],"Foley catheter",{"type":29,"name":36,"description":37,"armGroupLabels":38,"otherNames":39},"External Urinary Catheter","A non-sterile, external catheter intended for non-invasive urine output management",[24,19],[40],"PureWick",[42,47],{"name":43,"role":44,"phone":45,"phoneExt":10,"email":46},"Josh Hobson","CONTACT","484-790-4982","joshua.hobson@bd.com",{"name":48,"role":44,"phone":10,"phoneExt":10,"email":49},"Kirsten Hammitt","Kirsten.Hammitt@bd.com",[51],{"facility":52,"status":10,"city":53,"state":54,"zip":55,"country":56,"countryCode":57,"cosmosGeoPoint":58,"geoPoint":63,"contacts":10},"Intermountain Medical Center","Murray","Utah","84111","United States","US",{"type":59,"coordinates":60},"Point",[61,62],-111.88799,40.66689,{"lat":62,"lon":61},{"type":65,"investigatorFullName":10,"investigatorTitle":10,"investigatorAffiliation":10,"oldNameTitle":10,"oldOrganization":10},"SPONSOR",[67],{"name":68,"class":6},"Becton, Dickinson and Company","100650169","evaluation-of-male-and-female-external-catheters-for-urine-output-monitoring-in-the-icu-100650169",false,"NCT07744945","Evaluation of Male and Female External Catheters for Urine Output Monitoring in the ICU","A Prospective, Observational Pilot Study Evaluating the Performance and Clinical Acceptance of PureWick® When Used in the ICU for Urine Output Monitoring","Inclusion Criteria:\n\n1. Adult patients =18 years at the time of ICU admission\n2. Female and Male Patients requiring urine output monitoring\n3. Provision of a signed and dated informed consent form\n\nExclusion Criteria:\n\n1. Frequent episodes of bowel incontinence without a fecal management system in place; or\n2. Has moderate to heavy menstruation or vaginal bleeding and cannot use a tampon or menstrual cup; or\n3. Has urinary retention; or\n4. Is agitated, combative, restless, and\u002For uncooperative and may remove or dislodge the external catheter or indwelling catheter; or\n5. Presence of moderate to severe insensible fluid loss, including but not limited to: Diaphoresis; Anasarca; or, based on the investigator's assessment, is unlikely to provide accurate urine leakage measurements on the pad due to the presence of other fluids (e.g. blood, stool); or\n6. Any other condition that, in the opinion of the investigator, would preclude them from participating in the study","ALL","18 Years",{"count":79,"type":80},32,"ESTIMATED","OBSERVATIONAL","The goal of this observational pilot study is to learn about the ability of the PureWick® Flex Female External Catheter and the PureWIck® Male External Catheter to capture urine output in adult ICU patients compared to indwelling urinary catheters. The study will also gather feedback from ICU clinicians about the suitability of PureWick® urine output data to inform clinical decision-making.",[84,85],"Urine Output","ICU Patients","NOT_YET_RECRUITING","2026-07-31",{"date":89,"type":90},"2026-08-04","ACTUAL",{"date":92,"type":80},"2026-08",{"date":94,"type":80},"2026-10",{"name":5,"class":6},1]