Actively Recruiting

Phase 4
Age: 18Years +
All Genders
NCT04090359

Dual Mobility Acetabular Cups in Revision TJA

Led by Rush University Medical Center · Updated on 2026-05-05

322

Participants Needed

2

Research Sites

1000 weeks

Total Duration

On this page

Sponsors

R

Rush University Medical Center

Lead Sponsor

R

Rothman Institute Orthopaedics

Collaborating Sponsor

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Dual Mobility Acetabular Cups in Revision TJA

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patient is older than 18 years
  • Scheduled for revision total hip arthroplasty (THA), including revision of both components
  • Includes conversion of hip resurfacing or hemiarthroplasty to THA
  • Includes revision of single components allowing dual-mobility bearing implantation
  • Includes reimplantation following two-stage revision for periprosthetic infection
  • Acetabular shell diameter must accommodate at least a 36mm femoral head
Not Eligible

You will not qualify if you...

  • Younger than 18 years
  • Undergoing primary total hip arthroplasty (THA)
  • Conversion of non-arthroplasty femoral neck fracture fixation to THA
  • Unwilling to participate in the study
  • Surgeon decides intraoperatively to use a constrained liner

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 2 locations

1

New York University Medical Center

New York, New York, United States, 10003

Not Yet Recruiting

2

Rothman Institute

Philadelphia, Pennsylvania, United States, 19107

Actively Recruiting

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Research Team

C

Craig Della Valle, MD

CONTACT

A

Anne DeBenedetti, BA

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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