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

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Alexis wound retractor — DEVICE
    A surgical device used to retract tissue during procedures, designed to reduce wound trauma and improve healing
  • Standard wound retractor — DEVICE
    A 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 Retractor
    Subjects in this arm will undergo surgery using the Alexis wound retractor.
  • Active Comparator: Non-Alexis Retractor
    Subjects 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

Locations (1)

FacilityCityStateZIPSite coordinators
University of MiamiMiamiFlorida33125
Natalia Cruz, MD
3056895195

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