Wound Closure Materials and Techniques in Hip and Knee Arthroplasty

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age30+
SponsorBahattin Kemah

About this trial

This prospective randomized clinical study aims to evaluate the effects of different suture materials and wound closure techniques on wound healing, functional outcomes, and postoperative complications in patients undergoing total hip and knee arthroplasty.

A total of at least 90 adult patients undergoing primary or aseptic revision lower extremity arthroplasty will be randomized into two groups according to the wound closure material and technique used. All surgeries will be performed by the same surgical team following standardized operative protocols.

Primary outcomes include wound-related complications such as prolonged wound drainage, wound dehiscence, surgical site infection, and local inflammatory findings within 90 days postoperatively. Secondary outcomes include operative time, bleeding amount, cosmetic outcomes, and functional scores.

The results of this study are expected to help determine the most effective and safe wound closure method in lower extremity arthroplasty.

Eligibility criteria

Qualifiers

Age ≥ 30 years

Patients undergoing primary total hip arthroplasty or total knee arthroplasty

Patients undergoing aseptic revision total hip or knee arthroplasty

Surgery performed by the same surgical team

Disqualifiers

Age < 30 years

Patients receiving immunosuppressive therapy

Patients with complicated diabetes mellitus

Chronic venous insufficiency

Trial design

Treatments tested in this trial

  • Barbed Suture Wound Closure
  • Conventional Suture Wound Closure

Treatment groups

90 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Bahattin Kemah

Lead sponsor

Umraniye Education and Research Hospital

Sponsor institution