At a glance
ClinicalIndex Comparison RecordN/ACompleted· 160 enrolled
Drug / intervention
Prevenadevice
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.
Randomized Controlled Trial of Wound Management With Negative Pressure Dressing Versus Standard Dressing After Knee and Hip Revision Arthroplasty.
In Brief
A clinical study evaluating Prevena for Prosthesis-related Infections and 3 related conditions. Completed, enrolled 160 participants across 1 site.
Detailed Summary
The purpose of this study is to determine the efficacy of a negative pressure wound therapy (NPWT) system after revision total knee and hip arthroplasty in patients at high risk for infection. It is hypothesized that the use of NPWT system (i.e., Prevena) in high risk patients prevents wound complications and decreases reoperation rates.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsProsthesis-related Infections, Wound Complications, Joint Diseases, Musculoskeletal Diseases
CountriesUnited States
CollaboratorsKCI USA, Inc
Timeline
N/ACompletedFinished
2014201520162017201820192020202120222023202420252026
First PostedApr 2014
Enrollment StartMay 2014
Primary CompletionApr 2017
Study CompletionJun 2017
TodayJul 2026
First PostedApr 30, 2014
Enrollment StartMay 1, 2014
Primary CompletionApr 24, 2017
Study CompletionJun 30, 2017
TodayJul 2, 2026
Enrollment to primary: 3.0 yearsPosted 12.2 years ago
Interventions
Prevenadevice
Device will be applied at end of procedure over closed incision.