[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"catheter-associated-urinary-tract-infection\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:catheter-associated-urinary-tract-infection":67},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,6,0,[8,51,83,115,143,169],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":23,"conditions":24,"keywords":34,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":39,"lastUpdatePostDateStruct":40,"startDateStruct":43,"completionDateStruct":45,"leadSponsor":47,"locationsCount":50},"100624164","duke-virtual-integrated-workflow-100624164",false,"NCT07406074","Duke Virtual IntEgrated Workflow","DUH Innovation Units","Duke VIEW","Inclusion Criteria:\n\n* Admission to the hospital on one of six clinical units\n\nExclusion Criteria:\n\n* Less than 18 years old","ALL","18 Years",{"count":20,"type":21},10000,"ESTIMATED","OBSERVATIONAL","This quality improvement initiative aims to evaluate the implementation, utilization, and impact of virtual care technologies and workflows being implemented at Duke University Health System (DUHS). This project is embedded within operational workflows and is designed to inform strategic decision-making and resource allocation. The evaluation will focus on key performance indicators (KPIs) relevant to hospital operations and patient outcomes, including but not limited to: Length of Stay, Readmission Rates, Patient Satisfaction Scores, and Other Quality and Safety Metrics. These KPIs will be evaluated across three clinical units at Duke University Hospital, in which virtual care technologies are being implemented. These will be compared to three control units of similar characteristics. Differences in KPIs will be examined across all units over 12 months.",[25,26,27,28,29,30,31,32,33],"Falls Injury","Readmission Rates","CLABSI - Central Line Associated Bloodstream Infection","Catheter Associated Urinary Tract Infection","Hospital Acquired Pressure Injury","Venous Thromboembolism (VTE)","Nurses","Satisfaction, Patient","Length of Stay",[35,36,37],"Virtual Care","Nursing","Inpatient","NOT_YET_RECRUITING","2026-02-09",{"date":41,"type":42},"2026-02-12","ACTUAL",{"date":44,"type":21},"2026-02-04",{"date":46,"type":21},"2027-02-03",{"name":48,"class":49},"Duke University","OTHER",1,{"id":52,"slug":53,"hasResults":11,"nctId":54,"briefTitle":55,"officialTitle":56,"acronym":4,"eligibilityCriteria":57,"healthyVolunteers":11,"sex":58,"minAge":18,"maxAge":59,"enrollmentInfo":60,"targetDuration":4,"studyType":62,"phases":63,"briefSummary":65,"conditions":66,"keywords":68,"overallStatus":73,"whyStopped":4,"lastUpdateSubmitDate":74,"lastUpdatePostDateStruct":75,"startDateStruct":77,"completionDateStruct":79,"leadSponsor":81,"locationsCount":50},"100509419","phase-2-vitamin-c-effectiveness-in-preventing-urinary-tract-infections-after-gynecological-surgeries-100509419","NCT05913180","Vitamin C Effectiveness in Preventing Urinary Tract Infections After Gynecological Surgeries","Vitamin C for the Prevention of Catheter-associated Urinary Tract Infections in Women Who Undergo Elective Gynecological Surgeries: a Randomized Double-blinded Controlled Trial","Inclusion Criteria:\n\n* Nonpregnant women\n* 18 years of age or older\n* Undergoing elective GYN surgery\n\nExclusion Criteria:\n\n* Pregnant women\n* Already taking Vitamin C supplementation\n* Nephrolithiasis\n* Congenital anomaly or neurogenic bladder\n* Allergy to ascorbic acid\n* On therapeutic anticoagulant medicine during the 6 weeks after surgery\n* Gynecological surgery involving fistula repair or a vaginal mesh removal\n* Positive Urinalysis in the pre-admission unit\n* Recurrent UTIs\n* Diabetes\n* G6PD\n* Hemochromatosis\n* Renal disorders","FEMALE","80 Years",{"count":61,"type":21},180,"INTERVENTIONAL",[64],"PHASE2","Double-blind placebo-controlled randomized trial aiming to assess the role of Vitamin C supplementation in the prevention of catheter-associated urinary tract infections in women undergoing elective gynecological surgeries.",[67],"Catheter-Associated Urinary Tract Infection",[69,70,71,72],"Ascorbic acid","Vitamin C","Elective Gynecologic surgeries","CAUTI","RECRUITING","2025-12-23",{"date":76,"type":42},"2025-12-30",{"date":78,"type":42},"2023-09-19",{"date":80,"type":21},"2026-08-15",{"name":82,"class":49},"American University of Beirut Medical Center",{"id":84,"slug":85,"hasResults":11,"nctId":86,"briefTitle":87,"officialTitle":88,"acronym":4,"eligibilityCriteria":89,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":90,"enrollmentInfo":91,"targetDuration":4,"studyType":62,"phases":93,"briefSummary":95,"conditions":96,"keywords":100,"overallStatus":73,"whyStopped":4,"lastUpdateSubmitDate":106,"lastUpdatePostDateStruct":107,"startDateStruct":109,"completionDateStruct":111,"leadSponsor":113,"locationsCount":50},"100600126","adhesive-devices-versus-elastic-devices-for-urinary-catheter-securement-in-critically-ill-patients-experimental-study-100600126","NCT07093437","Adhesive Devices Versus Elastic Devices for Urinary Catheter Securement in Critically Ill Patients Experimental Study","Dispositivos Adhesivos Frente a Dispositivos elásticos Para la sujeción de la Sonda Urinaria en el Paciente crítico Estudio Experimental","Inclusion Criteria:\n\n* Age \\> 18 years\n* Pacients with an urinary catheter inserted within the past 24 hours\n* Expected duration of catheterization \\>48 hours\n* Estimated ICU lenght os stay \\> 48 hours\n\nExclusion Criteria:\n\n* Known allergy to adhesive tape\n* Patients with lesions at the urinary meatus, ongoing urinary tract infection or suspected infection\n* Presence of urological or prostatic pathology\n* Any condition that prevents securing the urinary catheter to the thigh, such as wounds, burns, or amputations","99 Years",{"count":92,"type":21},188,[94],"NA","Nowadays there are two types of urinary catheter securement devices, adhesive and elastic bands. The goal of this clinical trial is to determine which type of device-adhesive or elastic-is more effective for securing urinary catheters in critically ill patients. The study also aims to evaluate the prevention of urethral meatus injuries, patient discomfort, and the incidence of catheter-associated urinary tract infections .\n\nThe main questions the trial aims to answer are:\n\n* Which device type better prevents injuries to the urethral meatus?\n* Which device reduces discomfort for patients?\n* Which device lowers the incidence of catheter-associated urinary tract infections?\n\nParticipants will:\n\n* Use either an adhesive or an elastic device to secure their urinary catheter during their stay in critical care\n* Be monitored regularly to assess any injuries, discomfort, or infections related to the catheter\n* Provide feedback on their comfort and any complications experienced, if they are able to communicate",[97,98,67,99],"Pressure Injuries","Pain","Medical Device Site Injury",[101,102,103,104,105],"Urinary catheter securement","Urinary catheter fixation","Catheter-associated urinary tract infections","pain","Meatal pressure injuries","2025-12-03",{"date":108,"type":42},"2025-12-10",{"date":110,"type":42},"2025-09-22",{"date":112,"type":21},"2026-10-30",{"name":114,"class":49},"Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau",{"id":116,"slug":117,"hasResults":11,"nctId":118,"briefTitle":119,"officialTitle":120,"acronym":72,"eligibilityCriteria":121,"healthyVolunteers":11,"sex":122,"minAge":18,"maxAge":4,"enrollmentInfo":123,"targetDuration":4,"studyType":62,"phases":125,"briefSummary":126,"conditions":127,"keywords":130,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":135,"lastUpdatePostDateStruct":136,"startDateStruct":138,"completionDateStruct":139,"leadSponsor":141,"locationsCount":50},"100606222","the-effect-of-education-on-patients-attitudes-and-anxiety-towards-cauti-prevention-100606222","NCT07172750","The Effect of Education on Patients' Attitudes and Anxiety Towards CAUTI Prevention","The Effect of Education on Patients' Attitudes Towards Preventing Catheter-Associated Urinary Tract Infections and Anxiety After Urologic Surgery","Inclusion Criteria:\n\n* Age 18 and over,\n* Male patients,\n* Discharged with a urinary catheter after TURP, HOLEP, Internal Urethrotomy, and Open Prostatectomy surgeries at the urology department of the University Hospital where the study will be conducted,\n* Possess the cognitive, affective, and psychomotor skills to perform self-care (no coordination problems affecting the upper extremities),\n* Are literate,\n* Have no visual or auditory communication problems,\n* Have no previous psychiatric disorder\u002Fdiagnosis and are not currently taking medication for psychiatric disorders,\n* Individuals who volunteer to participate in the study will be included.\n\nExclusion Criteria:\n\n* Patients who are under 18 years of age,\n* Female patients,\n* Patients who have undergone surgeries other than TUR-P, HOLEP, Internal Urethrotomy, and Open Prostatectomy,\n* Patients with an oncological diagnosis and ongoing care\u002Ftreatment, or who have previously received oncological treatment,\n* Patients who develop postoperative complications\u002Fwhose general health deteriorates, who do not wish to participate in the study, or who wish to withdraw\u002Fexit from any aspect of the study will not be included in the study.","MALE",{"count":124,"type":21},70,[94],"This research will be carried out determine the effect of education given to patients after urological surgery on their attitudes and anxiety levels towards preventing catheter-related urinary tract infections.",[28,128,129],"Indwelling Urinary Catheter","Urologic Surgery",[131,132,133,129,134],"Catheter associated urinary tract infection","Anxiety","self-care","patient education","2025-09-08",{"date":137,"type":42},"2025-09-15",{"date":137,"type":21},{"date":140,"type":21},"2026-04-30",{"name":142,"class":49},"Istanbul University - Cerrahpasa",{"id":144,"slug":145,"hasResults":11,"nctId":146,"briefTitle":147,"officialTitle":148,"acronym":4,"eligibilityCriteria":149,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":150,"targetDuration":4,"studyType":62,"phases":152,"briefSummary":153,"conditions":154,"keywords":155,"overallStatus":73,"whyStopped":4,"lastUpdateSubmitDate":160,"lastUpdatePostDateStruct":161,"startDateStruct":163,"completionDateStruct":165,"leadSponsor":167,"locationsCount":50},"100588072","replace-the-impact-of-catheter-replacement-in-patients-with-catheter-associated-urinary-tract-infection-100588072","NCT06936631","REPLACE: The Impact of Catheter Replacement in Patients With Catheter-associated Urinary Tract Infection","REPLACE: the Impact of Catheter Replacement in Patients With Catheter-associated Urinary Tract Infection","Inclusion Criteria:\n\n1. Aged 18 years or older.\n2. An indwelling catheter, either a transurethral or suprapubic catheter, that has been in place for at least 2 weeks.\n3. At least one CAUTI-related symptom, defined according to the IDSA guideline (11): onset or worsening of fever (\\> 38 degrees), rigors, altered mental status, malaise or lethargy with no other identified cause, flank pain, costovertebral angle tenderness, acute haematuria, pelvic discomfort, or suprapubic pain\u002Ftenderness. In patients with spinal cord injury, increased spasticity, autonomic dysreflexia, or sense of unease are also compatible with CAUTI.\n4. Urine culture with ≥ 103 colony-forming units (CFU)\u002FmL of ≥ 1 bacterial species, or urine culture with \\\u003C103 CFU\u002FmL along with a positive blood culture with the same microorganism as the urine culture.\n5. The ability to provide written informed consent for the use of their data.\n6. Sufficient proficiency in the Dutch or English language, both spoken and written, to effectively communicate with the research team and accurately complete the questionnaires.\n\nExclusion Criteria:\n\n1. Having an immunodeficiency: High-dose corticosteroid use (any equivalent of ≥ 20 mg prednisolone per day for \\> 4 weeks), severe primary immunodeficiency, organ transplant, neutropenia (absolute neutrophil count \\\u003C 0.50 x 10⁹\u002FL)\n2. Expiration of the indication of the indwelling catheter.\n3. Having a planned (routine) catheter replacement during antibiotic therapy.\n4. Contraindications for catheter replacement (judgement treating physician)\n5. Kidney catheters (nephrostomy or double-J catheter).\n6. Needing bladder irrigations because of gross haematuria.\n7. Having bladder stones.\n8. Female patients who are pregnant.\n9. Having a life expectancy of \\\u003C 3 months.",{"count":151,"type":21},300,[94],"With this project the investigators aim to address the following question: \"Is it beneficial to change bladder catheters during urinary tract infections?\" There is debate regarding the usefulness of changing an indwelling catheter during antibiotic treatment of a catheter-associated urinary tract infection (CAUTI). The current guideline recommends catheter replacement, but is based on limited evidence. Our hypothesis is that there is no added value for patients to change the catheter during an antibiotic treatment for CAUTI. If refraining from catheter replacement is non inferior, this would result in a reduction of invasive procedures and reduction of healthcare associated costs. Patients with CAUTI and an indication for antibiotic treatment will be randomized to catheter replacement or no catheter replacement. The study will be conducted in academic and non-academic hospitals in The Netherlands. 300 patients will need to be included.",[28],[131,72,156,157,158,159],"Urinary tract infection","UTI","Indwelling catheter","Urosepsis","2025-04-22",{"date":162,"type":42},"2025-04-27",{"date":164,"type":21},"2025-04",{"date":166,"type":21},"2029-02",{"name":168,"class":49},"Leiden University Medical Center",{"id":170,"slug":171,"hasResults":11,"nctId":172,"briefTitle":173,"officialTitle":174,"acronym":175,"eligibilityCriteria":176,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":177,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":179,"conditions":180,"keywords":181,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":184,"lastUpdatePostDateStruct":185,"startDateStruct":187,"completionDateStruct":189,"leadSponsor":191,"locationsCount":4},"100586866","participant-satisfaction-and-quality-of-life-with-catheter-washouts-in-adults-living-with-long-term-catheters-and-currently-using-uro-tainer-polihexanide-002-100586866","NCT06920953","Participant Satisfaction and Quality of Life With Catheter Washouts in Adults Living With Long-Term Catheters and Currently Using Uro-Tainer® Polihexanide 0.02%","A Prospective Observational Study to Evaluate Participant Satisfaction and Quality of Life With Catheter Washouts in Adults Living With Long-Term Catheters and Currently Using Uro-Tainer® Polihexanide 0.02%","UTP Washout","Inclusion Criteria:\n\n* Male or female aged 18 years\n* Participant is having a urethral or suprapubic long-term catheter (LTC) in situ for more than 28 days and no plan for discontinuation of LTC at the time of recruitment\n* Currently using the LTC washout maintenance solution Uro-Tainer® Polihexanide 0.02%\n* Able to undertake LTC washouts or has a designated person (relative, friend, other informal carer, or paid\u002FNHS healthcare worker) able to perform washouts\n* Able to complete the study documentation or has a designated person able to assist with study documentation\n* Informed consent obtained\n\nExclusion Criteria:\n\n* Age younger than 18 years\n* Intermittent self catheterisation\n* Pregnant or contemplating pregnancy or breastfeeding\n* Ongoing S-CAUTI (until treatment is complete)\n* Visible haematuria (unless investigated\u002Ftreated)\n* Known allergies to the LTC washout solution\n* Current bladder cancer (until treatment is complete and participant discharged from cancer surveillance program)\n* Known bladder stones (until treatment is complete)\n* Not able to communicate or to give consent including participants with incapacity to consent\n* Any other clinical and social reasons that would be deemed by the recruitment team to be unsuitable for the study\n* Simultaneous participation in another clinical trial\n* in case of hypersensitivity (allergy) to PHMB, chlorhexidine, or excipient of the solution.\n* several days after surgery on the bladder or the urinary tract\n* for open wounds, the inner and middle ear, the central nervous systems, eyes, hyaline cartilage, and meninges",{"count":178,"type":21},50,"Uro-Tainer® Polihexanide 0.02% (acronym: UTP washout) is a sterile, single-use, water-based solution (100 ml) currently used in clinical practice in the UK (and Europe) for the irrigation of Long-Term-Catheter. This medical device is intended for the maintenance of indwelling urethral and suprapubic Long-Term-Catheter to aid removal of deposits, tissue waste, clots, and mucus.\n\nIn this study of people living with Long-Term-Catheter and currently using UTP washouts as part of their standard clinical care, the following will be investigated :\n\n* Participant satisfaction with their UTP washout\n* Impact of UTP washout plan on their QoL\n* Adverse events (blockage, SCAUTI, others)\n* Participant adherence to their current washout frequency plan. This is an observational study. The participants are those currently using UTP washouts as prescribed by their clinical care team. There will be no change in treatment for study purposes.",[28],[182,183],"Catheter Washouts","Suprapubic long-term catheter","2025-04-08",{"date":186,"type":42},"2025-04-10",{"date":188,"type":21},"2025-05-01",{"date":190,"type":21},"2026-02-28",{"name":192,"class":193},"B. Braun Ltd. Centre of Excellence Infection Control","INDUSTRY"]