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Non-returning Catheter Valve for Reducing CAUTI | Clinical Trials | Clareo Health

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COMPLETEDNANCT01963013

Non-returning Catheter Valve for Reducing CAUTI

This study was to determine efficacy of the non-returning catheter valve for reducing catheter associated urinary tract infection compared with conventional urine bag in critically ill patients.

Lead sponsor: Khon Kaen University•1 locations•View source on ClinicalTrials.gov

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Sponsors

Lead Sponsor

Khon Kaen University

Non-returning catheter valve (generic name) used UnometerTM SafetiTM Plus (trade name)

Age

18 - No limit years

Sex

ALL

Healthy Volunteers

No

Inclusion Criteria

•The participants who age more than 18 year and admitted to the medical intensive care unit or intermediate care unit
•All participants must be retained the urinary catheter.

Exclusion Criteria

•The participants were diagnosed urinary tract infection before retention of the urinary catheter.

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Data from ClinicalTrials.govLast updated on ClinicalTrials.gov: October 21, 2013Terms

Trial snapshot

StatusCOMPLETED

PhaseNA

Enrollment100

Start dateJun 2012

Last updatedOct 21, 2013

Condition

Catheter Associated Urinary Tract Infection Critically Ill Patients

Locations shown

Srinagarind hospital

Muang, Changwat Khon Kaen

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: October 21, 2013Data synced to Clareo: June 28, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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