Novel Device for Reducing Catheter-Related Infections

Status Withdrawn

Clinical Trial Summary

This study is a pilot study of the safety, tolerability and efficacy of an investigational central venous catheter device used in conjunction with a standard central venous catheter. The hypothesis is that utilization of a catheter device incorporating cyanoacrylate will reduce catheter colonization by bacteria, and may decrease the rate of catheter-related bloodstream infections.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Supportive Care

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT00878683
Study type	Interventional
Source	University of Kansas Medical Center
Contact
Status	Withdrawn
Phase	N/A
Start date	July 2009
Completion date	April 2011

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