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New hip implant under the microscope: will it last 10 years?
NCT ID NCT05366712
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study follows 125 adults aged 18-75 who are getting a hip replacement with a new type of implant (the Trident II shell). The main goal is to see how long the implant lasts without needing another surgery. Researchers will also track patients' pain and function using a standard hip score. The implant is already approved for use, but this study collects real-world data on its long-term performance.
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.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 125 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jun 2022
- Expected to finish
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Nov 2034
An estimate. End dates often move.
- Lead sponsor
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A government agency
The lead sponsor is a government body.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 75 years
- 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Patients undergoing planned primary total hip arthroplasty with standard implants, suitable for the use of the uncemented Trident® II acetabular component. 2. Patients aged 18-75 3. Patients willing and able to comply with the study protocol 4. Patients that provide informed consent Exclusion Criteria: 1. Patients not meeting study inclusion criteria 2. Bone stock that is inadequate for support or fixation of the prosthesis 3. Patients with a body mass index (kg/m2) \>40 4. Procedures performed for pain relief in those with severely restricted mobility
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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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NHS Lothian
Edinburgh, Lothian, EH16 4SA, United Kingdom
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Other studies related to the condition(s) this trial covers.
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