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.

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Key information

Conditions

Catheter Associated Urinary Tract Infection Critically Ill Patients

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Srinagarind hospital

Muang, Changwat Khon Kaen, 40002, Thailand

About this study

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

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Non-returning catheter valve

Device

Other names: UnometerTM SafetiTM Plus

Conventional urine bag

Device

Primary outcomes

Incidence density of the catheter associated urinary tract infection (CAUTI)

Time frame: one year

Sponsors and collaborators

Lead sponsor

Khon Kaen University

Other

Registry information

Official study title

A Pilot Study of Non-returning Catheter Valve for Reducing Catheter-associated Urinary Tract Infection in Critically-ill Patients

Important dates

Study start: 2012
Primary completion: 2013
Study completion: 2013
First posted: Oct 16, 2013
Registry last updated: Oct 21, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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