CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 41 enrolled
Drug / intervention
Air Barrier System devicedevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01559506
NCT01559506N/ACompleted
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ABS to Reduce Contamination in Spine Surgery

Nimbic Systems, LLC·interventional·Posted Mar 21, 2012·Updated Mar 17, 2015

In Brief

A clinical study evaluating Air Barrier System device for Surgery. Completed, enrolled 41 participants across 1 site.

Detailed 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

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsSurgery
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
201220132014201520162017201820192020202120222023202420252026
First PostedMar 21, 2012
Enrollment StartNov 1, 2011
Primary CompletionFeb 1, 2015
TodayJul 2, 2026
Enrollment to primary: 3.3 yearsPosted 14.3 years ago

Interventions

Air Barrier System devicedevice

Device is deployed adjacent to the surgery site and activated.