Status:
WITHDRAWN
Novel Device for Reducing Catheter-Related Infections
Lead Sponsor:
University of Kansas
Collaborating Sponsors:
University of Missouri-Columbia
Conditions:
Intensive Care
Eligibility:
All Genders
18+ years
Phase:
NA
Brief 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...
Eligibility Criteria
Inclusion
- 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
- 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
Key Trial Info
Start Date :
July 1 2009
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
April 1 2011
Estimated Enrollment :
Patients enrolled
Trial Details
Trial ID
NCT00878683
Start Date
July 1 2009
End Date
April 1 2011
Last Update
May 5 2015
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