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Improving the bearing surface in total hip replacement (THR): the use of oxidised zirconium and highly cross-linked polyethylene

Improving the bearing surface in total hip replacement (THR): the use of oxidised zirconium and highly cross-linked polyethylene - a randomised controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN48522433
Enrollment
200
Registered
2005-04-14
Start date
2009-01-14
Completion date
Unknown
Last updated
2016-10-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Arthritis of the hip Musculoskeletal Diseases Coxarthrosis

Interventions

Primary total hip replacement, using either cobalt chrome or oxinium femoral heads and either standard or highly cross-linked polyethylene liners.

Sponsors

University College London Hospitals NHS Trust (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. The patient and surgeon agree that primary THR is necessary 2. The patient is 18 years of age or older (either sex) on the day of signing the Study Consent Form 3. The patient is capable of participating in the study: 3.1. Fluent in English, or has a capable proxy 3.2. Mentally intact 3.3. Emotionally stable 3.4. A permanent resident in an area accessible to the study site

Exclusion criteria

Exclusion criteria: 1. Current medical conditions such as: 1.1. Metastatic or primary tumor of the hip 1.2. Implantation into a previously resected hip (i.e. conversion to THR) 1.3. Neurologic deficit impairing the affected limb 2. History of medical conditions such as: 2.1. Septic arthritis in the affected hip 2.2. Reflex sympathetic dystrophy of the affected leg 2.3. Progressive muscular condition causing deterioration of the abductor muscles 2.4. Hip pain associated with back pathology such as spinal stenosis or vascular occlusion

Design outcomes

Primary

MeasureTime frame
Radiographic wear; measuring linear & volumetric wear based on standardised AP & lateral radiographs of the pelvis then analysed with an automated edge detection technique

Secondary

MeasureTime frame
Not provided at time of registration

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026