Vitamin e in hip implants: a Longer-Lasting fix?
NCT ID NCT01713062
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 2 times
Summary
This study compares two types of hip implant liners—one with vitamin E and one without—to see which lasts longer and causes fewer problems like wear or bone damage. Researchers are following 400 adults aged 18 to 75 who need a hip replacement due to arthritis. The goal is to find out if the vitamin E liner reduces implant failure over time.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- hip implant liner (highly cross-linked polyethylene with or without vitamin E)
- What this could lead to
- If successful, this could show that adding vitamin E to hip implant liners reduces wear and extends implant life, improving outcomes for hip replacement patients.
- What could go wrong
- This is a long-term study still in progress, so results are not yet final. The benefit of vitamin E may be small or not apply to all patients, and implant failure or complications remain possible.
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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400 people
The number who actually took part.
- Started
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Jan 2012
- Expected to finish
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Jun 2030
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
adult patients
- 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.
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: * Minimum age: 18 years * Maximum age: 75 years * Indication of cementless THA * Approval of study participation and treatment according to study protocol * Physical and mental willingness of adhering to clinical and radiological follow up Exclusion: * Patient is not able to join follow up * Increased risk of anaesthesia according to the "American Society of Anesthesiology": ASA IV * Tumor disease * Alcohol and drug dependency * Permanent cortisone therapy * Clinical relevant infections * Pregnancy and planned pregnancy * Previous interventions like adjustment-osteotomy, treatment of fractures or THA on affected side * Acute fractures of the affected hip joint * Patients with bone quality, which doesn´t allow a cementless treatment * Requirements of clinical relevant deformities (condition after preoperation or bone fracture, leg length discrepancy \> 30 mm, Offset-reduction about \> 30 mm) * Small acetabular treatments with 28 mm heads * Treatments without using ceramic heads * Treatments which require neck prolonging components
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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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Elisabeth Klinikum Olsberg
Olsberg, 59939, Germany
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Fachklinik für Orthopädie, Unfallchirurgie, WirbelsäulenchirurgieMarienhaus Klinikum St. Josef
Bendorf, 56170, Germany
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Klinik für Orthopädie und Unfallchirurgie
Bochum, 44791, Germany
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Klinik und Poliklinik für Orthopädie
Halle, 06097, Germany
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Orthopädische Klinik der MHH im Annastift
Hanover, 30625, Germany
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St. Marien Hospital
Mülheim, Germany
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Other studies related to the condition(s) this trial covers.
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