Bikini vs Longitudinal Incision in Direct Anterior Approach (DAA) Total Hip Arthroplasty (THA)
Recruiting · NCT06831045 · Interventional (participants receive a specific treatment) · Lead sponsor: University of Miami
View the official record on ClinicalTrials.gov →Interventions studied
Bikini IncisionLongitudinal Incision
What this trial is about
The study team is conducting this study to see if there is a difference between the wound healing and participant satisfaction rates between two incision types used during a THA done via the DAA technique.
Who can take part
Age range
18 Years and older
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not applicable (e.g. observational or device study)
Study type
Interventional (participants receive a specific treatment)
Inclusion criteria
- Patients with body mass index greater than or equal to 30
- Patients undergoing primary unilateral DAA THA
- Patients undergoing primary THA
Exclusion criteria
- Patients with body mass index less than 30
- Patients with a history of prior open surgery on the affected hip
- Patients unable/unwilling to undergo spinal anesthesia under monitored anesthesia care (MAC)
- Patients with allergies or absolute contraindication to standardized drugs administered within the University of Miami protocol for total hip replacement
- The following groups will not be included: adults unable to consent, individuals who are not yet adults, pregnant women, prisoners.
Where it is running
1 location listed across 1 US state.
- University of Miami - Miami, Florida, United States