Novel Device for Reducing Catheter-Related Infections

University of Kansas

Overview

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.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

SUPPORTIVE_CARE

Masking

NONE

Conditions

Intensive Care

Interventions

silicone catheter bootDEVICE

silicone device using Dermabond

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Admission in the ICU at time of catheter insertion * Indication for central venous catheter placement * De novo catheter insertion in the subclavian or internal jugular veins Exclusion Criteria: * Anticipated catheter duration \< 72 hours * Planned guidewire exchange * Documented bacteremia within 48 hours prior to catheter placement * Extensive skin breakdown near the site of potential catheter placement * Emergent line placement * Screening labs with ANC \< 500 or platelets \< 50K * Hypersensitivity to cyanoacrylates or formaldehyde * Prior enrollment in study

Outcomes

Primary Outcomes

Catheter site inspection

Time frame: Baseline, Daily

Data from ClinicalTrials.gov

This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.