[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"urine-output\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:urine-output":24},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,1,0,[8],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":4,"briefSummary":22,"conditions":23,"keywords":4,"overallStatus":26,"whyStopped":4,"lastUpdateSubmitDate":27,"lastUpdatePostDateStruct":28,"startDateStruct":31,"completionDateStruct":33,"leadSponsor":35,"locationsCount":5},"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":19,"type":20},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.",[24,25],"Urine Output","ICU Patients","NOT_YET_RECRUITING","2026-07-31",{"date":29,"type":30},"2026-08-04","ACTUAL",{"date":32,"type":20},"2026-08",{"date":34,"type":20},"2026-10",{"name":36,"class":37},"C. R. Bard","INDUSTRY"]