Air Barrier System for the Prevention of Prosthesis-related Infections

Status Recruiting

Clinical Trial Summary

This is a prospective, randomized, blinded clinical trial to determine if the Air Barrier System device reduces the incidence of surgical site infection after total hip replacement, acetabular repair, posterior spinal fusion, and prosthetic vascular graft procedures.

Clinical Trial Description

This project is an evaluation of a novel device, the Air Barrier System (ABS), to reduce the risk of prosthesis-related surgical site infection in a multi-center clinical trial. The ABS shields surgical incisions intra-operatively by creating a field of high-purity air surrounding an incision that prevents airborne microorganisms from entering the incision.

This research will evaluate ABS performance in a prospective, randomized, blinded multi-center trial. The surgical procedures studied will include total hip arthroplasty, trauma-related acetabula reconstruction, posterior instrumented spine fusion, and prosthetic vascular graft procedures. Patients will be enrolled during the first two years of the study, and CDC guidelines require a one year follow-up period to monitor patients for potential prosthesis-related infections. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02376153
Study type	Interventional
Source	Nimbic Systems, LLC
Contact	Sean Self
Phone	281-565-5715
Email	self@nimbicsystems.com
Status	Recruiting
Phase	N/A
Start date	April 24, 2015
Completion date	October 2019

View Details

See also
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