Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
100 participants
INTERVENTIONAL
2012-06-30
2013-04-30
Brief Summary
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Detailed Description
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Conditions
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Keywords
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
NONE
Study Groups
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Non-returning catheter valve
Non-returning catheter valve (UnometerTM SafetiTM Plus) was used in experimental group only.
Non-returning catheter valve
Conventional urine bag
Conventional urine bag hasn't the non-returning catheter valve.
Conventional urine bag
Interventions
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Non-returning catheter valve
Conventional urine bag
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* All participants must be retained the urinary catheter.
Exclusion Criteria
18 Years
ALL
No
Sponsors
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Khon Kaen University
OTHER
Responsible Party
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Anupol Panitchote
Anupol Panitchote
Locations
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Srinagarind hospital
Muang, Changwat Khon Kaen, Thailand
Countries
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References
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Panitchote A, Charoensri S, Chetchotisakd P, Hurst C. Pilot study of a non-return catheter valve for reducing catheter-associated urinary tract infections in critically ill patients. J Med Assoc Thai. 2015 Feb;98(2):150-5.
Other Identifiers
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CAUTI-001
Identifier Type: -
Identifier Source: org_study_id