Study Results
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View full resultsBasic Information
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COMPLETED
83 participants
OBSERVATIONAL
2011-10-31
2012-05-31
Brief Summary
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Detailed Description
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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.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Ceramic on metal THA
Those who have received a ceramic on metal total hip replacement
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* 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
* Mentally infirm / incapacitated
* Incomplete history or physical examination
* Unwillingness to participate in the study
18 Years
ALL
No
Sponsors
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Hussain Kazi
OTHER
Responsible Party
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Hussain Kazi
Specialist Registrar, Trauma and Orthopaedics
Principal Investigators
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Fintan A Carroll, MBBS, FRCS
Role: STUDY_DIRECTOR
Consultant Orthopaedic Surgeon
Hussain A Kazi, MBChB,FRCS
Role: PRINCIPAL_INVESTIGATOR
Specialist Registrar, Trauma & Orthopaedics
Locations
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Wirral University Teaching Hospitals NHS Foundation Trust
Metropolitan Borough of Wirral, Merseyside, United Kingdom
Countries
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Other Identifiers
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960558216
Identifier Type: -
Identifier Source: org_study_id
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