Surgery Clinical Trial
Official title:
A Clinical Study to Compare the CAUTI Rates Following ERASE CAUTI Tray Non-Silver Coated Foley Catheters Verse Silver Coated Foley Catheters
Verified date | September 2016 |
Source | Medline Industries |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Food and Drug Administration |
Study type | Observational |
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.
Status | Terminated |
Enrollment | 756 |
Est. completion date | September 2016 |
Est. primary completion date | September 2016 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
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. |
Observational Model: Cohort, Time Perspective: Prospective
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Medline Industries |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in Urinary tract infection rates | Infection rate/1000 catheter days. | 3-9 months based on size of ICU and catheter usage | Yes |
Secondary | Catheter use | Number of days catheters used. | Catheter days | No |
Secondary | Infection Costs | Catheter related charges for infections | Duration of infection | No |
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