At a glance
ClinicalIndex Comparison RecordN/ACompleted· 29 enrolled
Drug / intervention
Air Barrier System Device +1 moredevice
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 Particulate in the Surgical Field Using Directed Local Airflow
In Brief
A clinical study evaluating Air Barrier System Device and Sham Air Barrier System device for Surgery. Completed, enrolled 29 participants across 1 site.
Detailed Summary
The objective of this study is to determine whether the Air Barrier System device reduces airborne particulate and airborne colony forming units present at a surgery site.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsSurgery
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
200920102011201220132014201520162017201820192020202120222023202420252026
Enrollment StartMay 2009
Primary CompletionSep 2009
First PostedSep 2009
TodayJul 2026
First PostedSep 4, 2009
Enrollment StartMay 1, 2009
Primary CompletionSep 1, 2009
TodayJul 2, 2026
Enrollment to primary: 4 monthsPosted 16.8 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 surgery site.
Sham Air Barrier System devicedevice
Device is deployed to the surgery site, but the airflow is not activated. This intervention is used to determine any effects that the presence of the device alone may have.