NCT02127281.
Methods | Randomised controlled trial |
Participants | Patients with a scheduled revision total hip or knee arthroplasty procedure |
Interventions | PREVENA versus control |
Outcomes | Number of participants with wound complications; reoperation rates; readmission rates; knee flexion; HOOS and KOOS scores at 90 days postoperatively; timed‐up‐and‐go test; hip range of motion (flexion); VR‐12 questionnaire; hip range of motion; knee extension |
Notes |