Dual Mobility Acetabular Cups in Revision TJA
ConditionDislocation, Hip
Trial statusRecruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age18+
SponsorRush University Medical Center
About this trial
The aim of this study is to the compare clinical outcomes of patients undergoing a revision total hip arthroplasty (THA) with the use of a dual mobility bearing versus a single bearing design with the use of a large femoral head (36mm or 40mm). We hypothesize the use of dual-mobility components in revision THA will be associated with a lower dislocation rate in the first year following surgery.
Eligibility criteria
Qualifiers
Any patient older than 18 years of age scheduled for a revision THA, including revision of both components, conversion of a hip resurfacing to THA, conversion of a hemiarthroplasty to THA, and revision of single components which allow implantation of dual-mobility bearings. In addition, patients undergoing reimplantation of a total hip arthroplasty following a two-stage revision for periprosthetic infection will also be included. Only patients with an acetabular shell diameter capable of accommodating at least a 36mm femoral head will be included.
Disqualifiers
Less than 18 years of age, primary THA,
conversion of non-arthroplasty femoral neck fracture fixation to THA,
patients unwilling to participate.
patients where the surgeon makes the intraoperative decision to use a constrained liner will be excluded.
Trial design
Treatments tested in this trial
- Dual Mobility Implant
- Conventional, single-bearing implant
Treatment groups
322 Participants
are divided into 2 treatment groupsLocations
2New York University Medical Center10003, New YorkNew York, United States
Rothman Institute19107, PhiladelphiaPennsylvania, United States
Sponsors and collaborators
Rush University Medical Center
Lead sponsor
Rothman Institute Orthopaedics
Collaborator
Keck School of Medicine of USC
Collaborator
NYU Langone Health
Collaborator
Source ClinicalTrials.gov