Study to Compare CAUTI Rates Following ERASE CAUTI Tray Non-Silver vs Silver Coated Foley Catheters

A Clinical Study to Compare the CAUTI Rates Following ERASE CAUTI Tray Non-Silver Coated Foley Catheters Verse Silver Coated Foley Catheters

Status

Terminated

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT02101762

Enrollment

756

Registered

2014-04-02

Start date

2014-05-31

Completion date

2016-09-30

Last updated

2016-09-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Intensive Care Units, Surgery

Keywords

Foley, Catheters, CAUTI, ERASE CAUTI

Brief summary

The Foley catheter is one component in a catheter insertion procedure that could contribute to a catheter associated urinary tract infection (CAUTI). Improvement in the catheter insertion procedures using the ERASE CAUTI Tray system may help to lower these infection rates.

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Inclusion criteria

* At least 18 years of age * Received Either silver coated Foley catheter or ERASE CAUTI non-silver coated catheter

Exclusion criteria

* UTI present upon current hospital admission * Burn patients, transplant patients, or immune-compromised patients.

Design outcomes

Primary

Measure	Time frame	Description
Change in Urinary tract infection rates	3-9 months based on size of ICU and catheter usage	Infection rate/1000 catheter days.

Secondary

Measure	Time frame	Description
Catheter use	Catheter days	Number of days catheters used.
Infection Costs	Duration of infection	Catheter related charges for infections

Outcome results