Study to Compare CAUTI Rates Following ERASE CAUTI Tray Non-Silver vs Silver Coated Foley Catheters
NCT ID: NCT02101762
Last Updated: 2016-09-13
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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TERMINATED
756 participants
OBSERVATIONAL
2014-05-31
2016-09-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Silver Coated Catheters
Subjects that had previously received silver coated Foley catheters.
No interventions assigned to this group
ERASE CAUTI Non-Silver Coated Catheters
Subjects that received non-silver catheters from an ERASE CAUTI tray.
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Received Either silver coated Foley catheter or ERASE CAUTI non-silver coated catheter
Exclusion Criteria
* Burn patients, transplant patients, or immune-compromised patients.
18 Years
ALL
No
Sponsors
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Medline Industries
INDUSTRY
Responsible Party
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Principal Investigators
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Ed Drower, MS
Role: STUDY_DIRECTOR
Medline Industries
Other Identifiers
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MII-001
Identifier Type: -
Identifier Source: org_study_id
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