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ACTIVE NOT RECRUITING
NCT04092634
PHASE4

Dual Mobility in "High Risk" Patients

Sponsor: Rush University Medical Center

View on ClinicalTrials.gov

Summary

The aim of this study is to compare clinical outcomes of patients considered to be high risk for prosthetic dislocation undergoing primary total hip arthroplasty (THA) with the use of a dual mobility bearing versus a conventional, single bearing design.

Official title: Dual-mobility vs. Single-bearing Components in THA at "High Risk" for Prosthetic Dislocation

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

412

Start Date

2017-11-01

Completion Date

2035-02-01

Last Updated

2025-06-26

Healthy Volunteers

No

Interventions

DEVICE

Dual mobility implant

Patients that are eligible and consent to the study will be randomized to receive either a dual mobility implant or a traditional single-bearing hip implant. This group is for the dual mobility implant

DEVICE

Traditional, Single-bearing hip implant

Patients that are eligible and consent to the study will be randomized to receive either a dual mobility implant or a traditional single-bearing hip implant. This group is for the dual mobility implant

Locations (4)

Keck School of Medicine of USC

Los Angeles, California, United States

Rush University Medical Center

Chicago, Illinois, United States

New York University Medical Center

New York, New York, United States

Rothman Orthopaedic Institute

Philadelphia, Pennsylvania, United States