Clinical Trials Directory

Trials / Terminated

TerminatedNCT00872794

A Single Centre Study to Assess the Long-term Performance of the DePuy ASR™ System in Primary Hip Resurfacing Surgery

Prospective Single-centre, Uncontrolled, Post Marketing Surveillance Study to Monitor the Long-term Performance of the DePuy ASR™ Hip in Subjects With Suitable Indications for a Primary Resurfacing Hip Arthroplasty

Status
Terminated
Phase
Phase 4
Study type
Interventional
Enrollment
50 (actual)
Sponsor
DePuy International · Industry
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to monitor the performance and determine the metal ion release of the DePuy ASR™ System in the treatment of patients with hip joint disease requiring hip resurfacing surgery. Patients who enter the study will be evaluated at regular intervals following hip surgery using patient, clinical and x-ray assessments. A subset of patients will also have blood samples taken at regular intervals to allow the metal ion levels to be determined and undergo scans to allow the bone mineral density of the bone surrounding the implant to be monitored. DePuy decided to close this Study in 4Q 2009. The Study was terminated with effect from November 2010 to allow for the completion of the 5 year follow up assessments. Please note that subsequent to this decision DePuy voluntarily recalled the ASR products on 24 August 2010. Additional information regarding this voluntary recall and the follow-up of patients affected by the recall can be found at the following links http://www.mhra.gov.uk/Publications/Safetywarnings/MedicalDeviceAlerts/CON079157 and http://www.depuy.com/countries\_list.

Conditions

Interventions

TypeNameDescription
DEVICEDePuy ASR™ Hip SystemA metal-on-metal bearing surface replacement system for use in resurfacing hip arthroplasty.

Timeline

Start date
2003-11-01
Primary completion
2010-05-01
Completion
2010-05-01
First posted
2009-03-31
Last updated
2017-06-26

Locations

1 site across 1 country: South Africa

Source: ClinicalTrials.gov record NCT00872794. Inclusion in this directory is not an endorsement.