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New hip implant shows promise in 10-Year study
NCT ID NCT02648152
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study followed 218 people who received a cementless POLARSTEM hip implant to treat osteoarthritis. Researchers tracked how well the implant worked and how long it lasted over up to 10 years. The goal was to see if this implant is a safe and effective option for hip replacement.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Cementless POLARSTEM hip implant
- What this could lead to
- If successful, this could confirm that the POLARSTEM implant is a reliable, long-lasting option for hip replacement in people with osteoarthritis.
- What could go wrong
- This is an observational study, not a controlled trial, so results may not apply to all patients. Some implants may fail or require revision over time.
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
-
218 people
The number who actually took part.
- Started
-
Mar 2009
- Finished
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Nov 2020
- 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
Patients enrolled in this multicenter clinical observation will have at least one of the indications listed below and meet all of the inclusion criteria. Patients meeting any of the exclusion criteria are not eligible for this study. Indications * Primary or secondary coxarthrosis * Rheumatoid arthritis * Developmental dysplasia of the hip (Crowe type I and II) * Fracture or avascular necrosis of the femoral head
- Ages
-
18 to 75 years
- Sex
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Anyone
- Healthy volunteers
-
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: * Patient has no general medical contraindication to surgery * Informed consent to participate in the MCO signed by the patient * Routine radiographic assessment is possible * Patient is likely to comply with study follow-up requirements * Primary total hip replacement (THR) to the affected side, unilateral or bilateral Exclusion Criteria: * Previously failed endoprosthesis and /or THR components in relevant hip * History of infection in the affected joint; systemic infections * Grossly insufficient femoral or acetabular bone stock in the involved hip * Charcot joint disease or other severe neurosensory deficit * Severe spinal disorders * Age of patient at date of surgery \> 75 years * High comorbidity * Cemented acetabular cup
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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
-
Kantonsspital Aarau, Orthopedics
Aarau, 5001, Switzerland
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St. Elisabeth Hospital, Orthopedics and Rheumatology
Bochum, 44787, Germany
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University Marburg, Orthopedics and Rheumatology
Marburg, Germany
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