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Contact the study team using the details below to take part. If there are no contact details below please ask your doctor in the first instance.

Contact Information:

NAZ IQBAL
nazalie.iqbal1@nhs.net


NAZ IQBAL
nazalie.iqbal1@nhs.net


Mr David Langton
Djlangton22@doctors.org.uk


Raghavendra Sidaginamale
r.sidaginamale1@nhs.net


Study Location:

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Be Part of Research - Trial Details - Removal joint replacement

Removal joint replacement

Medical Conditions

Complications of surgical and medical care, not elsewhere classified


This information is provided directly by researchers, and we recognise that it isn't always easy to understand. We are working with researchers to improve the accessibility of this information. In some summaries, you may come across links to external websites. These websites will have more information to help you better understand the study.


The production of prosthetic joints that will consistently outlive the patient remains the ultimate goal of arthroplasty. Conventional metal on polyethylene hip replacements have proven, reliable results but are less successful in younger, active patients. This is because polyethylene wear debris can stimulate a cascade of events leading to osteolysis, loosening and joint failure. It has been shown that this process is directly related to the volume of wear debris produced at the articulating surface. Failure of a joint replacement leads to removal and a new replacement to be fitted. This is termed a “revision.” Revision surgery is more challenging than primary hip replacement for both surgeon and patient. There is a significantly increased mortality rate and, even if the procedure goes uneventfully, dislocation rates have been reported to be as high as 30%.

For this reason, a number of different bearing surface combinations have been tried in an attempt to increase the longevity of hip replacements. These combinations include ceramic on ceramic, ceramic on polyethylene, ceramic on metal and metal on metal. Our previously approved protocol focused on the study of failed metal on metal hips. In this ongoing study we have shown that a number of these types of hips wear at a much greater rate than expected. This accelerated wear can leave the patient at risk of local complications including bone, nerve and muscle damage. Unfortunately we have identified a particular problem at the junction of the femoral head and the femoral stem. This is commonly termed the “taper junction”. We suspect that industry wide design modifications which have taken place in the last ten are putting other conventional types of hips at risk of taper failure.
We would therefore like to study all types of hip replacements at our centres in Newcastle University, University of Surrey, Freeman Hospital, University Hospital of North Tees. Furthermore, the routine analysis of more types of hips will allow us to determine which types of bearing materials are associated with the lowest wear rates.

Apart from issues related to wear, prosthetic hips also have a much greater risk of dislocation. Dislocation is incredibly painful and distressing and can become a recurrent problem requiring revision surgery. Again, patients are told to avoid putting their legs in particular “at risk” positions, positions which are not beyond those of activities of normal daily living. The analysis of failed hip replacements in conjunction with the assessment of the position in which the component was placed in the pelvis will allow us to explore the link between dislocation and component orientation in a large number of patients with the added knowledge that wear analysis will provide to this area of investigation.

Start dates may differ between countries and research sites. The research team are responsible for keeping the information up-to-date.  

The recruitment start and end dates are as follows:

21 Aug 2009 30 Apr 2026

Observational

Observational type: Validation of investigation /therapeutic procedures;



You can take part if:



You may not be able to take part if:


No exclusion criteria.


Below are the locations for where you can take part in the trial. Please note that not all sites may be open.

  • Northwick Park Hospital
    Harrow
    Middlesex
    HA1 3UJ
  • University College Hospital
    London
    Greater London
    NW1 2BU
  • University Hospital (coventry)
    Coventry
    West Midlands
    CV2 2DX
  • Southampton General Hospital
    Southampton
    Hampshire
    SO16 6YD
  • The James Cook University Hospital
    Middlesbrough
    Cleveland
    TS4 3BW
  • Southmead Hospital
    Bristol
    Avon
    BS10 5NB
  • University Hospital Of North Durham
    Durham
    County Durham
    DH1 5TW
  • University Hospital Of North Tees
    Stockton-on-tees
    Cleveland
    TS19 8PE
  • University Hospital Of Hartlepool
    Hartlepool
    Cleveland
    TS24 9AH
  • Ealing Hospital
    Southall
    Middlesex
    UB1 3HW
  • Central Middlesex Hospital
    London
    Greater London
    NW10 7NS
  • Broadgreen Hospital
    Liverpool
    L14 3LB

NAZ IQBAL
nazalie.iqbal1@nhs.net


Mr David Langton
Djlangton22@doctors.org.uk


Raghavendra Sidaginamale
r.sidaginamale1@nhs.net


NAZ IQBAL
nazalie.iqbal1@nhs.net



The study is sponsored by NORTH TEES AND HARTLEPOOL NHS FOUNDATION TRUST and funded by BRITISH ORTHOPAEDIC FOOT & ANKLE SOCIETY .




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for Trial ID: CPMS 40478

Last updated 19 August 2025

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