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COMPLETEDNANCT00972153

Device to Reduce Surgery Site Contamination

The objective of this study is to determine whether the Air Barrier System device reduces airborne particulate and airborne colony forming units present at a surgery site.

Lead sponsor: Nimbic Systems, LLC•1 U.S. locations•View source on ClinicalTrials.gov

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Sponsors

Lead Sponsor

Nimbic Systems, LLC

The Air Barrier System 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 Air Barrier System can reduce the presence of airborne colony-forming units (e.g. bacteria colonies) and particulate at the surgery site.

Age

All ages

Sex

ALL

Healthy Volunteers

No

Inclusion Criteria

•Candidate for primary total hip arthroplasty

Exclusion Criteria

•Prior history of infection
•Revision arthroplasty
•Screens positive for MRSA
•Undergoing hemiarthroplasty or resurfacing

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Data from ClinicalTrials.govLast updated on ClinicalTrials.gov: March 16, 2012Terms

Trial snapshot

StatusCOMPLETED

PhaseNA

Enrollment29

Start dateMay 2009

Last updatedMar 16, 2012

Condition

Locations shown

Texas Orthopedic Hospital

Houston, Texas

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: March 16, 2012Data synced to Clareo: June 28, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

View ClinicalTrials.gov Terms and Conditions