Actively Recruiting
Influence of Antiseptic Washes on Wound Healing Complications After THA
Led by F. Johannes Plate · Updated on 2026-02-05
420
Participants Needed
2
Research Sites
116 weeks
Total Duration
On this page
Sponsors
F
F. Johannes Plate
Lead Sponsor
I
Irrimax Corporation
Collaborating Sponsor
AI-Summary
What this Trial Is About
The purpose of this research trial is to evaluate the effect of two types of washing solutions on wound healing after total hip replacement surgery. Washing solutions are used routinely during total hip replacements to clean the wound after the components have been placed and the wound is about to be closed with sutures. It is currently not known which washing solution may be better for wound healing and whether a certain solution decreases the risk of wound healing complications after total hip replacement. Therefore, this research trial is being conducted. Study participants will be randomized into one of two groups: washing the surgical wound with povidone-iodine solution (Surgiphor, Becton Dickinson, Franklin Lakes, NJ) or chlorhexidine solution (Irrisept, Irrimax Corporation, Lawrenceville, GA). All patients will undergo standard of care total hip replacements without any other change in surgery. The best type of solution that cleans the wound and potentially leads to better wound healing is unknown. This study will evaluate whether there is difference in surgical wound healing between the two washing solutions. The study will pay for the washing solutions. Patients will follow up for standard postoperative visits. At the 2-week and 6-week visits, pictures of the surgical incision will be taken and saved in the electronic medical record and evaluated in a standardized way for healing of the incision and the appearance of the scar. Postoperative complications and returns to the hospital or additional surgeries will be collected from the electronic medical record.
CONDITIONS
Official Title
Influence of Antiseptic Washes on Wound Healing Complications After THA
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosis of osteoarthritis or avascular necrosis of the femoral head
- Failed conservative management and indicated for total hip replacement
You will not qualify if you...
- Known allergy to chlorhexidine or povidone-iodine
AI-Screening
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Trial Site Locations
Total: 2 locations
1
UPMC East
Monroeville, Pennsylvania, United States, 15146
Actively Recruiting
2
UPMC Shadyside
Pittsburgh, Pennsylvania, United States, 15232
Actively Recruiting
Research Team
F
Frank J Plate, MD, PhD
CONTACT
D
Dana Farrell, BS,PMP
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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