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Clinical Trial Summary

The 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 shoulder 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 and particles at the surgery site during total arthroplasty surgery. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03782675
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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