- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01437124
Metal Ions in Ceramic on Metal Total Hip Arthroplasty (COM)
Measurement of Metal Ion Levels and Chromosome Abnormalities in Ceramic on Metal Total Hip Arthroplasty in Vivo
Study Overview
Status
Detailed Description
PURPOSE & DESIGN:
The investigators are currently following up a cohort of patients all of whom have had a metal on ceramic total hip arthroplasty.
This new bearing couple has been approved for use in the UK for some time and has recently achieved USA FDA approval.
The attraction of this bearing couple is a low rate of wear with reduced complications associated with ceramic on ceramic bearing such as bearing fracture.
Of recent media attention has been the unacceptably high failure of the DePuy ASR metal on metal hip resurfacing. This metal on metal bearing couple has been associated with increased ion levels and chromosome abnormalities in vivo.
In vitro studies and small in vivo studies have revealed much lower wear, particle numbers and ion levels in ceramic on metal studies than in metal on metal bearing surfaces; however there is no large scale evidence that this is the case.
The investigators currently are following up the largest worldwide series of ceramic on metal bearings and clinical results are excellent. It is important however to obtain hard data on metal ion levels in this population firstly to ensure the long term function and health of this cohort but also to provide a barometer for other surgeons who will be using a prosthesis that as yet has little in the way of long term follow up and data on ion levels in a large cohort.
If the ion levels are unacceptably high then the investigators will need to follow these patients closely and offer revision surgery if there are clinical concerns.
For similar reasons it is important to monitor for chromosomal abnormalities.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
Merseyside
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Wirral, Merseyside, United Kingdom, CH49 5PE
- Wirral University Teaching Hospitals NHS Foundation Trust
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Over 18 years of age
- Complete history and physical examination
- Previously performed ceramic on metal total hip replacement
- An understanding of the purpose of the study and signed consent form
Exclusion Criteria:
- Hip arthroplasty other than ceramic on metal bearing
- Mentally infirm / incapacitated
- Incomplete history or physical examination
- Unwillingness to participate in the study
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
|
Ceramic on metal THA
Those who have received a ceramic on metal total hip replacement
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Cobalt Chromium Levels
Time Frame: 2 years post THR
|
Serum cobalt chromium levels post THR
|
2 years post THR
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Chromosomal Abnormality
Time Frame: 2 years post THR
|
Deviation of karyotype from normal 2 years post THR
|
2 years post THR
|
Collaborators and Investigators
Sponsor
Investigators
- Study Director: Fintan A Carroll, MBBS, FRCS, Consultant Orthopaedic Surgeon
- Principal Investigator: Hussain A Kazi, MBChB,FRCS, Specialist Registrar, Trauma & Orthopaedics
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 960558216
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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