At a glance
ClinicalIndex Comparison RecordN/ACompleted· 23 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.
Reduction of Airborne Microbes in the Surgical Field During Spine Procedures Using Directed Local Airflow
In Brief
A clinical study evaluating Air Barrier System Device for Surgery. Completed, enrolled 23 participants across 1 site.
Detailed 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.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsSurgery
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
20102011201220132014201520162017201820192020202120222023202420252026
Enrollment StartNov 2009
Primary CompletionOct 2010
Study CompletionDec 2010
First PostedDec 2010
TodayJul 2026
First PostedDec 17, 2010
Enrollment StartNov 1, 2009
Primary CompletionOct 1, 2010
Study CompletionDec 1, 2010
TodayJul 2, 2026
Enrollment to primary: 11 monthsPosted 15.5 years ago
Interventions
Air Barrier System Devicedevice
Device is deployed adjacent to the surgery site and activated so that the filtered air emits over the site.