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ENROLLING BY INVITATION
NCT05548972
NA

G7 Dual Mobility With Vivacit-E or Longevity PMCF

Sponsor: Zimmer Biomet

View on ClinicalTrials.gov

Summary

This study is a global, multi-center, prospective, non-controlled, non-randomized, post-market clinical follow-up study. The main objectives of this study are to confirm the long-term safety, performance, and clinical benefits of the G7 Dual Mobility Acetabular System when used with the Vivacit-E or Longevity polyethylene hip bearing and instrumentation in primary total and revision (total) hip arthroplasty

Official title: Global, Multicenter and Prospective Post-Market Clinical Follow-Up Study of the G7® Dual Mobility Acetabular System With Vivacit-E® or Longevity® Poly Bearing & Instrumentation

Key Details

Gender

All

Age Range

18 Years - 80 Years

Study Type

INTERVENTIONAL

Enrollment

358

Start Date

2023-03-20

Completion Date

2037-08

Last Updated

2025-06-15

Healthy Volunteers

No

Interventions

DEVICE

G7 Dual Mobility with Vivacit-E bearing

hip arthroplasty with G7 Dual Mobility Vivacit-E bearing

DEVICE

G7 Dual Mobility Longevity bearing

hip arthroplasty with G7 Dual Mobility Longevity bearing

Locations (10)

Bowen Hefley Orthopedics

Little Rock, Arkansas, United States

HCA HealthONE Orthopedic Specialists

Denver, Colorado, United States

Jersey City Medical Center

Jersey City, New Jersey, United States

Hospital for Special Surgery

New York, New York, United States

The Cleveland Clinic

Cleveland, Ohio, United States

Slocum Research & Education Foundation

Eugene, Oregon, United States

UZ Leuven

Leuven, Belgium

Istituto San Siro

Milan, Italy

Pusan National University Yangsan Hospital

Yangsan, Gyeongsangnam, South Korea

Chonnam National University Hwasun Hospital

Hwasun, Jeollanam-do, South Korea