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Novel Device for Reducing Catheter-Related Infections

NCT00878683 · Status: WITHDRAWN · Phase: NA · Type: INTERVENTIONAL

Last updated 2015-05-05

No results posted yet for this study

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.

Conditions

  • Intensive Care

Interventions

DEVICE

silicone catheter boot

silicone device using Dermabond

Sponsors & Collaborators

  • University of Missouri-Columbia

    collaborator OTHER

  • University of Kansas

    lead OTHER

Principal Investigators

  • Stephen Waller, MD · University of Kansas Medical Center

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-07-31
Primary Completion
2011-04-30
Completion
2011-04-30

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00878683 on ClinicalTrials.gov