Hip implant under observation: will it last?
NCT ID NCT03456622
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study is following 230 adults who received a G7 hip replacement system to see how long the implant lasts and how well it works. Participants have hip problems like arthritis or bone death. The study does not test a new treatment but simply watches and records outcomes over time.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
-
230 people
The number who actually took part.
- Started
-
Nov 2015
- Expected to finish
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Dec 2030
An estimate. End dates often move.
- Lead sponsor
-
A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
All individuals who receive the study device, meet inclusion/exclusion criteria and provided nformed consent.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Male and female ≥18 years * Non-inflammatory degenerative joint disease including osteoarthritis and avascular necrosis, suitable for unilateral primary hip replacement; * Rheumatoid arthritis; * Correction of functional deformity; * Voluntary written Informed Consent obtained Exclusion Criteria Pre-operative: * Prospect for recovery to independent mobility compromised by known coexistent medical problems; * Requiring revision hip replacement; * Requiring bilateral hip replacement; * Previous hip replacement (resurfacing or THR) on the contralateral side and whose outcome is achieving an Oxford Hip score \<18 points; * Likely post-operative leg length inequality \>5cm; * Neuromuscular disease affecting hip (Parkinson's, cerebral palsy, other spasticity); * Primary or metastatic tumour involving this hip; * Loss of abductor musculature, poor bone stock, or poor skin coverage around the hip joint; * Previous organ transplant; * Previous arthrodesis or excision arthroplasty * Abnormal acetabulum: * Acetabular deficiency - \>2cm superior loss acetabular dome or \>1.5cm protrusion acetabulae or wall deficiency\> half a wall; * Dysplasia (DDH) with \>2.5cm subluxation or complete dislocation; * Body mass index \> 40kg/m2; * Active or previous or suspected infection in this hip; * Sepsis or osteomyelitis; * Known sensitivity to device materials; * Women judged by the investigator to be of childbearing potential who are pregnant, nursing, or planning to become pregnant, and those who do not agree to remain on an acceptable method of birth control throughout the entire study period; * Unable to provide informed consent (insufficient English, cognitive disorder such as dementia, psychiatric illness); * Unable to complete follow-ups (life expectancy \<5 years, insufficient English, lives overseas, unable to return easily). Intra-operative: * Abnormal abductor mechanism - trochanter escape \> 1.5cm or gluteus medius totally non-functional or trochanter absence; * Unavailability of required size of prosthesis; * Abnormal acetabulum: * Acetabular deficiency - \>2cm superior loss acetabular dome or \>1.5cm protrusion acetabulae or wall deficiency\> half a wall; * Dysplasia (DDH) with \>2.5cm subluxation or complete dislocation.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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The Royal Bournemouth Hospital
Bournemouth, BH7 7DW, United Kingdom
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