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

Sponsor

DePuy International (Industry)

Overall Status

Terminated

CT.gov ID

NCT00208377

Collaborator

(none)

228

Enrollment

Locations

Arm

Duration (Months)

Patients Per Site

0.9

Patients Per Site Per Month

Study Details

Study Description

Brief 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 December 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.

Condition or Disease	Intervention/Treatment	Phase
Rheumatoid Arthritis Osteoarthritis Post-traumatic Arthritis Collagen Disorders Avascular Necrosis Nonunion of Femoral Fractures Congenital Hip Dysplasia Slipped Capital Femoral Epiphysis	Device: DePuy ASR Hip System	Phase 4

Study Design

Study Type:

Interventional

Actual Enrollment :

228 participants

Allocation:

N/A

Intervention Model:

Single Group Assignment

Masking:

None (Open Label)

Primary Purpose:

Treatment

Official Title:

Prospective Multi-Centre, Uncontrolled, Post Marketing Surveillance Study to Monitor the Long-Term Performance of the DePuy ASR Hip System in Subjects With Suitable Indications for a Primary Resurfacing Hip Arthroplasty

Study Start Date :

Jul 1, 2003

Actual Primary Completion Date :

Dec 1, 2010

Actual Study Completion Date :

Dec 1, 2010

Arms and Interventions

Arm	Intervention/Treatment
Other: DePuy ASR Hip System A metal-on-metal bearing surface replacement system for use in resurfacing hip arthroplasty	Device: DePuy ASR Hip System A metal-on-metal bearing surface replacement system for use in resurfacing hip arthroplasty

Arm

Intervention/Treatment

Other: DePuy ASR Hip System

A metal-on-metal bearing surface replacement system for use in resurfacing hip arthroplasty

Device: DePuy ASR Hip System

A metal-on-metal bearing surface replacement system for use in resurfacing hip arthroplasty

Outcome Measures

Primary Outcome Measures

Kaplan-Meier survivorship calculated annually [Annually]

Secondary Outcome Measures

UCLA Activity Score [3 months, 6 months and then annually]
WOMAC Score [3 months, 6 months and then annually]
Activity Assessment [3 months, 6 months and then annually]
Harris Hip Score [3mths, 1yr, 2 yrs, 5yrs, 10yrs and 15yrs post-surgery]
Radiographic analysis [pre-discharge, 3mths, 1yr, 2 yrs, 5yrs, 10yrs and 15yrs post-surgery]
Metal ion analysis in whole blood [3mths, 1yr, 2yrs and 5yrs post surgery]
Bone mineral density (DEXA) [pre-discharge, 3mths, 1yr, 2yrs and 5yrs post-surgery]

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years to 65 Years

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

Male or female subjects, aged between 18 and 65 years inclusive.
Subjects with current indications for standard metal-on-metal (MoM) hip resurfacing arthroplasty suitable for cementless fixation in the acetabulum. These include pain, deformity, and loss of function, which are not responsive to medical treatment.
Subjects who are able to give voluntary, written informed consent to participate in this investigation and from whom consent has been obtained.
Subjects, who, in the opinion of the Investigator, are able to understand this investigation, co-operate with the investigational procedures, and are willing to return to the hospital for all the required post-operative follow-ups.

Exclusion Criteria:

Subjects who, in the opinion of the Investigator, have an existing condition that would compromise their participation and follow-up in this study.
Subjects with proven significant osteoporosis and poor bone quality.
Subjects with compromised renal function.
Subjects with proven metal sensitivity.
Subjects with infectious, highly communicable diseases, which may limit follow-up i.e. active tuberculosis, hepatitis, immuno-compromised conditions, etc.
Women who are pregnant.
Subjects who are known drug or alcohol abusers or with psychological disorders that could affect follow-up care or treatment outcomes.
Subjects who have participated in a clinical study with an investigational product in the last 6 month(s).
Subjects who are currently, or have been in the last 12 months, participating in a clinical study which involves exposure to ionising radiation.
Subjects who are currently involved in any injury litigation claims.