Air Barrier System for the Prevention of Prosthesis-related Infections
Status unconfirmed · Not applicable
Conditions studied: Prosthesis-Related Infections
In brief
This is a prospective, randomized, blinded clinical trial to determine if the Air Barrier System device reduces the incidence of surgical site infection after total hip replacement, acetabular repair, posterior spinal fusion, and prosthetic vascular graft procedures.
Key facts
- Study ID
- NCT02376153
- Run by
- Nimbic Systems, LLC
- People needed
- 816
- Starts
- 2015-04-24
- Expected to finish
- 2019-10-01
- Last updated by the study team
- 2018-09-06
Who can join
Age: 21 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Total hip arthroplasty;
- Acetabular repair with instrumentation;
- Posterior lumbar, cervical, or thoracic (up to and including 6 vertebral levels) spine fusion with instrumentation and vascular prosthetic graft implantation.
You may not qualify if…
- History of prior prosthesis infection;
- Active infection;
- Open traumatic wounds as is the case after some acetabular fractures.
Where it is running
- Michael E. DeBakey VA Medical Center — Houston, Texas, United States (enrolling)
Full record on ClinicalTrials.gov
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