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Air Barrier System Device to Reduce Contamination in Posterior Spine Surgery

NCT01559506 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 41

Last updated 2015-03-17

Study results available
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Summary

The objective of this study is to determine whether the Air Barrier System (ABS) reduces airborne colony-forming units (e.g. bacteria) present at surgery sites during posterior spinal procedures

Conditions

  • Surgery

Interventions

DEVICE

Air Barrier System device

Device is deployed adjacent to the surgery site and activated.

Sponsors & Collaborators

  • Nimbic Systems, LLC

    lead INDUSTRY

Principal Investigators

  • Rabih O Darouiche, MD · Baylor College of Medicine

  • Sean Self · Nimbic Systems

Study Design

Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-11-30
Primary Completion
2015-02-28
Completion
2015-02-28

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 NCT01559506 on ClinicalTrials.gov