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Device to Reduce Surgery Site Contamination - Spine

NCT01262105 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 23

Last updated 2012-04-11

Study results available
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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 spinal procedures.

Conditions

  • Surgery

Interventions

DEVICE

Air Barrier System Device

Device is deployed adjacent to the surgery site and activated so that the filtered air emits over the site.

Sponsors & Collaborators

  • Nimbic Systems, LLC

    lead INDUSTRY

Principal Investigators

  • David Wimberley, MD · Fondren Orthopaedic Group

Study Design

Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
DOUBLE
Model
PARALLEL

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-11-30
Primary Completion
2010-10-31
Completion
2010-12-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01262105 on ClinicalTrials.gov