Alexis Retractor in Total Hip Arthroplasty

Starting soon · Not applicable

Conditions studied: Hip Osteoarthritis, Hip Arthritis

In brief

To determine if there is a difference in wound healing and surgical site infection (SSI) rates using the Alexis wound retractor vs. not using it in longitudinal direct anterior approach total hip arthroplasty.

Key facts

Study ID

NCT07237737

Run by

University of Miami

People needed

202

Starts

2026-12-01

Expected to finish

2028-01-01

Last updated by the study team

2026-02-05

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patients undergoing primary unilateral longitudinal direct anterior approach total hip arthroplasty
• Patients undergoing primary total hip arthroplasty

You may not qualify if…

• Patients with history of prior open surgery on the affected hip
• Patients with history of prior total hip arthroplasty on the contralateral hip
• Patients with allergies or absolute contraindication to standardized drugs administered within the University of Miami protocol for total hip replacement

Where it is running

• University of Miami — Miami, Florida, United States

Full record on ClinicalTrials.gov

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