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ACTIVE NOT RECRUITING
NCT05366712
NA

Nexus Evaluation Primary Trident II Uncemented Shell

Sponsor: NHS Lothian

View on ClinicalTrials.gov

Summary

This is a prospective cohort study assessing the survival of a new acetabula component which is based on the original Trident acetabular system (cementless shell) which is used for Total Hip Arthroplasty. The manufacturer recently introduced the evolution of this product, the Trident® II acetabular shell which was launched in 2017. This implant is CE marked and is now widely available for the UK market, however has minimal clinical outcomes data to support its use. As part of a stepwise introduction of devices to orthopaedic practice. This study will report the 10 year implant survival and patient functional outcomes of this new implant.

Official title: Nexus Evaluation Primary Trident II UNcemented shEll (NEPTUNE): A Longitudinal Cohort Study of the Hydroxyapatite Coated Trident II Acetabular System in Total Hip Arthroplasty

Key Details

Gender

All

Age Range

18 Years - 75 Years

Study Type

INTERVENTIONAL

Enrollment

125

Start Date

2022-06-01

Completion Date

2034-11-25

Last Updated

2026-02-13

Healthy Volunteers

No

Interventions

DEVICE

Stryker Trident® II HA coated cementless acetabula component

New acetabula component.

Locations (1)

NHS Lothian

Edinburgh, Lothian, United Kingdom