An Observational, Multinational, In Hospital Evaluation of Catheter Utilization Rates in Female Patients Using Indwelling Urinary Catheters and the PureWick™ Flex Female External Catheter Across Europe and the Middle East
NCT07798128 · Status: NOT_YET_RECRUITING · Type: OBSERVATIONAL · Enrollment: 240
Last updated 2026-09-01
Summary
Urinary catheterization is commonly used in hospitalized patients for the management of urinary incontinence, immobilization, and monitoring of urinary output. However, indwelling urinary catheters (IUCs) are associated with clinically significant risks, including catheter-associated urinary tract infections (CAUTIs), other infectious and non-infectious complications, prolonged hospital stay, and increased healthcare costs. The risk of complications increases with the duration of catheterization, highlighting the need for strategies to reduce unnecessary catheter use and minimize catheter dwell time.
The PureWick™ Female External Catheter (FFEC) is a non-invasive urine collection device designed to manage urinary incontinence in female patients without the need for an indwelling catheter. By providing an alternative approach to urinary management, it has the potential to reduce reliance on IUCs and associated complications while improving patient comfort and quality of care.
This study is a prospective, multinational, observational, sequential two-cohort study conducted in hospitalized adult female patients across Europe and the Middle East. The study aims to evaluate the effect of introducing the PureWick™ FFEC into clinical practice on indwelling urinary catheter utilization rates in routine hospital care.
Approximately 240 adult female patients requiring urinary management for incontinence during hospitalization will be enrolled across multiple clinical sites. The study consists of two sequential cohorts within participating sites. In Cohort 1, patients will receive standard care using indwelling urinary catheters only. In Cohort 2, following the introduction of the PureWick™ FFEC, patients will be managed using either the external catheter alone or in combination with indwelling catheters, according to routine clinical practice.
The primary objective is to compare indwelling urinary catheter utilization rates before and after the introduction of the PureWick™ FFEC. Catheter utilization is defined as the proportion of inpatient days during which an indwelling catheter is used (catheter-days per patient-days).
Secondary objectives include assessment of the occurrence and nature of adverse events, including urinary tract infections, catheter-associated urinary tract infections, incontinence-associated dermatitis, and falls, as well as evaluation of hospital length of stay. Exploratory objectives include assessment of patient and healthcare professional experience, device usability and satisfaction, pain and discomfort, and sleep quality.
Participants will be followed from enrollment until hospital discharge or up to 40 days, whichever occurs first. The results of this study are intended to provide real-world evidence on urinary catheter utilization patterns and to inform clinical practice regarding the role of non-invasive urinary management strategies in hospitalized female patients.
Conditions
- Urinary Incontinence
- Limited Mobility
Interventions
- DEVICE
-
PureWick™ Flex Female External Catheter (FFEC)
A non-invasive external urine collection device used for management of urinary incontinence in hospitalized female patients. The device is applied externally and connected to low-pressure suction for urine collection. It is used according to routine clinical practice, either as first-line management or following use of an indwelling urinary catheter.
- DEVICE
-
Indwelling Urinary Catheter (IUC)
An internal urinary catheter inserted into the bladder to allow continuous drainage of urine, used as part of standard of care in hospitalized patients. Type and model may vary according to institutional practice.
Sponsors & Collaborators
-
Becton, Dickinson and Company
lead INDUSTRY
Eligibility
- Min Age
- 18 Years
- Sex
- FEMALE
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2026-11-06
- Primary Completion
- 2027-06-30
- Completion
- 2027-08-31
More Related Trials
-
Bacteriuria and Indwelling Urinary Catheter.
NCT05039203 ·Status: ACTIVE_NOT_RECRUITING
-
Use of the VasoNova VPS System During PICC Placement in an Algorithm Confirmation Study Using Fluoroscopy
NCT01232933 ·Status: COMPLETED ·Phase: NA
-
Effectiveness of a Zinc Oxide Adhesive Securement Device in the Fixation of Midline and Peripherally Inserted Central Catheters in Hospitalized Adult Patients
NCT06770374 ·Status: RECRUITING ·Phase: NA
-
Tunneled Peripherally Inserted Central Catheter (PICC) in Adult Patients and Associated Outcomes
NCT06365528 ·Status: RECRUITING ·Phase: NA
-
Comparison of an Antibiotic Impregnated PICC Catheter Versus a Regular PICC Catheter in a Tertiary Care Setting
NCT01765738 ·Status: WITHDRAWN ·Phase: PHASE2
-
Reuse of Intermittent Urethral Catheters
NCT02129738 ·Status: COMPLETED ·Phase: NA
-
Reducing Catheter-Related Bloodstream Infections in the ICU With a Chlorhexidine-Impregnated Sponge (BIOPATCH)
NCT00548132 ·Status: COMPLETED ·Phase: PHASE4
-
Peripherally Inserted Central Catheter Insertion Site and Complication Rate in Neonates
NCT03474978 ·Status: RECRUITING ·Phase: NA
-
Advanced Dressings for CVC Infection Prevention in PICU
NCT07175116 ·Status: COMPLETED ·Phase: NA
-
Prospective Observational Study of the Power PICC Family of Devices and Accessories
NCT04263649 ·Status: COMPLETED
-
Comparison Between Initial Routine PICC and General IV Access in Terminally Ill Cancer Patients
NCT03299868 ·Status: COMPLETED ·Phase: PHASE2
-
Comparison of Central and Peripheral Venous Catheters
NCT00122707 ·Status: COMPLETED ·Phase: NA
-
Study of Complication Rates Associated With PICC for Left vs Right
NCT01638702 ·Status: COMPLETED ·Phase: NA
-
Local Inflammation Does Not Correlate With Bacterial Colonization and Contamination of Perineural Catheters
NCT02599181 ·Status: COMPLETED ·Phase: NA
-
Complications Associated With Central Venous Access in the NSICU: PICC vs CVC
NCT02314520 ·Status: COMPLETED ·Phase: NA
-
Peripherally Inserted Central Catheter (PICC) Thrombosis: Reverse Taper Versus Non-tapered Catheters
NCT00728819 ·Status: COMPLETED ·Phase: NA
-
Non-returning Catheter Valve for Reducing CAUTI
NCT01963013 ·Status: COMPLETED ·Phase: NA
-
Venous Site for Central Catheterization
NCT01479153 ·Status: COMPLETED ·Phase: NA
-
Comparison of Early Phase Infections Risk Between Midline and Piccline Caheters: MIDLINE AND PICCLINE CATHETERS
NCT05264402 ·Status: UNKNOWN
-
Peripherally Inserted Central Catheter Placement by IV Team Nurses Using the Sonic Flashlight
NCT00226226 ·Status: COMPLETED ·Phase: PHASE1
-
Evaluation of Tissue Glue on PICC and Midline Catheters Insertion Sites
NCT04900740 ·Status: UNKNOWN ·Phase: NA
-
PEEZY Midstream Urine Device Compared to Catheterized Urine Sample
NCT03729336 ·Status: COMPLETED ·Phase: NA
-
Betadine Bladder Irrigations vs. Standard of Care Prior to Indwelling Catheter Removal
NCT03447639 ·Status: TERMINATED ·Phase: PHASE4
-
Analysis of Microbial Biofilms in Peripheral Venous Catheters and Their Implication in Infectious Risk
NCT07258862 ·Status: NOT_YET_RECRUITING
-
Arrow Chloragard Peripherally-Inserted Central Catheters (PICC) Study
NCT03019302 ·Status: UNKNOWN ·Phase: NA