Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Mayo Clinic
Age
18–any
Sex
ALL
Healthy volunteers
Accepted
You may be eligible if
Scheduled to undergo primary total hip (via direct anterior approach, press-fit components) or total knee arthroplasty (via manual approach, cemented components).
Willing to comply with all study-related procedures and be available for the duration of the study.
Provide signed and dated informed consent.
You may not be if
Unable to provide signed and dated informed consent.
Unwilling or unable to comply with all study-related procedures.
Known history of sensitivity or allergic reaction to any of the study products or its components, including any products used for standard of care (such as dressings or any coverings).
Has underlying condition or state that, in the 'investigator's opinion, would make them too critically ill to complete the day 90 postoperative follow ups.
Pregnant, planning to become pregnant, or nursing female subjects.
Subject with any mental impairment or condition that would make them unable to properly consent without use of LAR or additional subject protections.
Subject is a prisoner and/or part of a vulnerable subject population, which necessitates additional human research subject protections beyond the scope of this protocol.
Subject with an active infection or systemic antibiotic therapy within 2 weeks prior to surgery with the exception of preoperative antimicrobial prophylaxis.
