Expired Study
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Minneapolis, Minnesota 55404


Purpose:

To assess blood stream infections in participants using two FDA-cleared devices: ClearGuard HD end caps compared to the Tego® connector with the CurosTM for Tego disinfecting port protector.


Study summary:

Prospective, cluster-randomized, open-label, post market, comparative effectiveness evaluation with facilities participating for up to 13 months.


Criteria:

Inclusion Criteria: - All patients dialyzing with a central venous catheter Exclusion Criteria: - Known allergy to chlorhexidine


NCT ID:

NCT02593149


Primary Contact:

Principal Investigator
Steven M Brunelli, MD, MSCE
DaVita Clinical Research / DaVita HealthCare Partners


Backup Contact:

N/A


Location Contact:

Minneapolis, Minnesota 55404
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: November 18, 2019

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