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Clinical Trial Summary

This objective of this study is to determine whether the Air Barrier System device reduces airborne colony-forming units (e.g., bacteria) present at a surgery site during total knee arthroplasty surgeries.


Clinical Trial Description

The Air Barrier System (ABS) is a device that uses localized clean air flow to shield a surgery site from ambient airborne contamination. This study examines the hypothesis that the ABS can reduce the presence of airborne CFU at the surgery site during total knee arthroplasty surgery. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03473405
Study type Interventional
Source Nimbic Systems, LLC
Contact Gregory Stocks, MD
Phone 713-799-8600
Email stocks@fondren.com
Status Not yet recruiting
Phase N/A
Start date February 2019
Completion date July 2019

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