Alexis Retractor in Total Hip Arthroplasty
Part of paid clinical trials in Miami, Florida.
- Sponsor
- University of Miami
- Study ID
- NCT07237737
- Status
- Not Yet Recruiting
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Conditions
- Hip Arthritis
- Hip Osteoarthritis
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Alexis wound retractor — DEVICEA surgical device used to retract tissue during procedures, designed to reduce wound trauma and improve healing
- Standard wound retractor — DEVICEA conventional surgical retractor used during procedures without the features of the Alexis device
Study Details
To determine if there is a difference in wound healing and surgical site infection (SSI) rates using the Alexis wound retractor vs. not using it in longitudinal direct anterior approach total hip arthroplasty.
Key Dates
- Start date
- Dec 31, 2026
- Status verified
- Feb 2026
- Primary completion
- Jan 31, 2028
- Completion
- Jan 31, 2028
Study Design
- Enrollment
- 202 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Alexis RetractorSubjects in this arm will undergo surgery using the Alexis wound retractor.
- Active Comparator: Non-Alexis RetractorSubjects in this arm will undergo surgery using a standard retractor that does not include the Alexis device.
Primary Outcome Measure
Number of Days to Identification of Delayed Wound Healing [ Time Frame: Up to 14 days ]
Central Contacts
- Natalia Cruz, MD305-689-5195
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| University of Miami | Miami | Florida | 33125 |
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