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ACTIVE NOT RECRUITING
NCT03371212
PHASE4

A Prospective Randomized Controlled Trial of Dual-Mobility Components in Primary THA

Sponsor: Rush University Medical Center

View on ClinicalTrials.gov

Summary

The aim of this study is to determine if the use of a modular dual mobility bearing is associated with clinically important increases in serum metal levels.

Official title: A Prospective Randomized Trial of Modular Dual Mobility Acetabular Components Versus Conventional Single Bearing Components in Primary Total Hip Arthroplasty

Key Details

Gender

All

Age Range

18 Years - 80 Years

Study Type

INTERVENTIONAL

Enrollment

52

Start Date

2017-12-15

Completion Date

2036-12-01

Last Updated

2026-01-08

Healthy Volunteers

No

Interventions

DEVICE

Dual mobility cohort

Patients will receive the Taperloc femoral stem, ceramic femoral head (size 32mm for acetabular components 48/50mm; size 36mm for acetabular components \> 52mm), polyethylene bearing, and G7 acetabular shell.

DEVICE

Conventional cohort

Patients will receive a Taperloc femoral stem, ceramic femoral head (size 32mm for acetabular components 48/50mm; size 36mm for acetabular components \> 52mm), polyethylene bearing, and G7 acetabular shell

Locations (1)

Rush University Medical Center

Chicago, Illinois, United States