Clinical Decision Support to Reduce Catheter Associated Urinary Tract Infections
Public ClinicalTrials.gov record NCT06454500. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Official title
Randomized, Controlled Evaluations of the Effectiveness of Clinical Decision Support Systems (REEDS)
Brief summary
Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.
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.
Study identification
- NCT ID
- NCT06454500
- Recruitment status
- Completed
- Study type
- Interventional
- Phase
- Not applicable
- Enrollment
- 79,369 participants
Conditions and interventions
Eligibility (public fields only)
- Age range
- 18 Years and older
- Sex
- All
- Healthy volunteers
- Accepts healthy volunteers
This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.
Study timeline
- Start date
- Aug 16, 2021
- Primary completion
- Apr 3, 2023
- Completion
- Apr 3, 2023
- Last update posted
- Jun 19, 2024
2021 – 2023
United States locations
- U.S. sites
- 8
- U.S. states
- 1
- U.S. cities
- 5
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| NewYork-Presbyterian Westchester | Bronxville | New York | 10708 | — |
| NewYork-Presbyterian Brooklyn Methodist Hospital | Brooklyn | New York | 11215 | — |
| NewYork-Presbyterian Hudson Valley Hospital | Cortlandt Manor | New York | 10567 | — |
| NewYork-Presbyterian Queens | Flushing | New York | 11355 | — |
| NewYork-Presbyterian Columbia University Irving Medical Center | New York | New York | 10032 | — |
| NewYork-Presbyterian Allen Hospital | New York | New York | 10034 | — |
| NewYork-Presbyterian Lower Manhattan Hospital | New York | New York | 10038 | — |
| NewYork-Presbyterian Weill Cornell Medical Center | New York | New York | 10065 | — |
Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT06454500, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
- What this page does not do
- No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
- Where the data comes from
- Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
- Last refresh
- Last update posted Jun 19, 2024 · Synced Sep 11, 2026
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Open the official record
The complete protocol, eligibility criteria, and contact information for NCT06454500 live on ClinicalTrials.gov.