New hip implant tracked for 10 years – will it last?
NCT ID NCT05822505
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study follows 280 adults aged 18–75 who received a new type of hip implant (MonoCer cup) during a total hip replacement. Researchers will check how long the implant lasts without needing replacement, and measure pain, function, and satisfaction over 2, 5, and 10 years. The goal is to see if this implant performs as well as or better than other options already approved.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 280 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jan 2021
- Expected to finish
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Jun 2032
An estimate. End dates often move.
- Lead sponsor
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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
At least 280 patients will be recruited who will have the Mpact 3D Metal MonoCer acetabular cup prosthesis from four surgeons in Australia.
- Ages
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18 to 75 years
- Sex
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Anyone
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: * Patients undergoing a primary total conventional hip replacement and are suitable for cementless acetabular cup according to the indications for use (On-label use). * Use of the Medacta Mpact 3D Metal MonoCer acetabular cup prosthesis. * Adults aged between 18 and 75 years at the time of registration. * Ability to give informed consent. * Patients who are informed of the conditions of the study and are willing to participate for the length of the prescribed follow-up period. Exclusion Criteria: Exclusion Criteria * Rheumatoid arthritis. * Patients with a history of active infection. * Any case not described in the inclusion criteria. * Revision procedures.
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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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Melbourne Orthopaedic Group
Melbourne, Australia
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Other studies related to the condition(s) this trial covers.
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