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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06454500
Other study ID # AAAU3416
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 17, 2021
Est. completion date April 4, 2023

Study information

Verified date June 2024
Source Columbia University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The goal of this randomized controlled trial is to compare the effects of a clinical decision support tool consisting of a 48-hour stop order for indwelling urinary catheters versus no clinical decision support in hospitalized patients with indwelling urinary catheters. The main questions it aims to answer are: - Does the presence of an automated stop order integrated as part of a clinical decision support tool reduce dwell time of urinary catheters and the rate of catheter associated urinary tract infections? Participants who have indwelling urinary catheters ordered will be randomized to either have these orders automatically expire after 48 hours unless an action is taken or have orders without expiration. Researchers will compare the urinary catheter dwell time and the rate of catheter associated urinary tract infections between the two groups.


Recruitment information / eligibility

Status Completed
Enrollment 79369
Est. completion date April 4, 2023
Est. primary completion date April 4, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Admitted to hospital - At least 18 years old - Has order placed for indwelling urinary catheter Exclusion Criteria: - Indication for urinary catheter labeled as either "Chronic" or "Placed by urology"

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Clinical decision support
A 48 hour expiration on orders placed for indwelling urinary catheters.

Locations

Country Name City State
United States NewYork-Presbyterian Westchester Bronxville New York
United States NewYork-Presbyterian Brooklyn Methodist Hospital Brooklyn New York
United States NewYork-Presbyterian Hudson Valley Hospital Cortlandt Manor New York
United States NewYork-Presbyterian Queens Flushing New York
United States NewYork-Presbyterian Allen Hospital New York New York
United States NewYork-Presbyterian Columbia University Irving Medical Center New York New York
United States NewYork-Presbyterian Lower Manhattan Hospital New York New York
United States NewYork-Presbyterian Weill Cornell Medical Center New York New York

Sponsors (1)

Lead Sponsor Collaborator
Columbia University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Urinary catheter dwell time The time between urinary catheter insertion and removal Measured from time of catheter insertion until catheter removal or hospital discharge if the catheter was not removed, up to 250 days.
Secondary Catheter Associate Urinary Tract Infection (CAUTI) rate The number of CAUTI's per 1000 catheter days. CAUTIs were defined according to NHSN (National Healthcare Safety Network) criteria as a urinary tract infection where an indwelling urinary catheter (IUC) was in place for more than two consecutive days in an inpatient location on the date of event or the day before, with day of device placement being Day 1. All positive urine cultures are reviewed by members of Infection Prevention and Control to determine if they meet the defined criteria for CAUTI. Events verified as CAUTIs are then recorded in the hospital data registry. The hospital data registry was used to determine CAUTI events in this study. The development of a CAUTI was assessed from time of catheter insertion until either catheter removal or hospital discharge if the catheter was not removed, up to 250 days.
Secondary CAUTI population rate The number of CAUTI's per 10000 hospital days CAUTIs were defined according to NHSN (National Healthcare Safety Network) criteria as a urinary tract infection where an indwelling urinary catheter (IUC) was in place for more than two consecutive days in an inpatient location on the date of event or the day before, with day of device placement being Day 1. All positive urine cultures are reviewed by members of Infection Prevention and Control to determine if they meet the defined criteria for CAUTI. Events verified as CAUTIs are then recorded in the hospital data registry. The hospital data registry was used to determine CAUTI events in this study. The development of a CAUTI was assessed from time of catheter insertion until either catheter removal or hospital discharge if the catheter was not removed, up to 250 days.
Secondary CAUTI Free survival The time a catheter "survived" before developing a CAUTI CAUTIs were defined according to NHSN (National Healthcare Safety Network) criteria as a urinary tract infection where an indwelling urinary catheter (IUC) was in place for more than two consecutive days in an inpatient location on the date of event or the day before, with day of device placement being Day 1. All positive urine cultures are reviewed by members of Infection Prevention and Control to determine if they meet the defined criteria for CAUTI. Events verified as CAUTIs are then recorded in the hospital data registry. The hospital data registry was used to determine CAUTI events in this study. The development of a CAUTI was assessed from time of catheter insertion until either catheter removal or hospital discharge if the catheter was not removed, up to 250 days.
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