Alexis O-Ring and Charnley Retrievers and Its Effect on Contamination on Total Hip Arthroplasty
NCT: NCT07621250 · COMPLETED
Brief Summary
Randomized, prospective, single-blind clinical trial comparing two static wound retractors - the Charnley retractor and the Alexis O-Ring retractor - in primary total hip arthroplasty (THA). The primary objective is to compare surgical site contamination rates between the two devices. Secondary objectives include comparison of incision length, surgical time, intraoperative skin lesions, and postoperative complications including periprosthetic joint infection. Patients will be randomized 1:1 to either retractor group. Surgical site contamination will be assessed through four intraoperative cultures taken at standardized timepoints. Follow-up will be conducted at 1 month postoperatively.
Frequently Asked Questions
What is Alexis O-Ring and Charnley Retrievers and Its Effect on Contamination on Total Hip Arthroplasty?
Alexis O-Ring and Charnley Retrievers and Its Effect on Contamination on Total Hip Arthroplasty is a clinical trial registered under NCT07621250. Current status: COMPLETED.
What is the status of NCT07621250?
The current status of NCT07621250 (Alexis O-Ring and Charnley Retrievers and Its Effect on Contamination on Total Hip Arthroplasty) is: COMPLETED.
When did Alexis O-Ring and Charnley Retrievers and Its Effect on Contamination on Total Hip Arthroplasty start?
Alexis O-Ring and Charnley Retrievers and Its Effect on Contamination on Total Hip Arthroplasty started on 2024-04-20.
Related Devices
Official Source
View on ClinicalTrials.gov →Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.