Which hip implant lasts longer? a Head-to-Head trial aims to find out
NCT ID NCT06870123
First seen Aug 12, 2026 · Last updated Aug 13, 2026 · Updated 1 time
Summary
This trial is testing two different cup designs for total hip replacement, both paired with the same stem, to see which one gives patients better hip function and less pain. About 120 people with hip arthritis or related conditions will be randomly assigned to receive either the Delta TT or Delta ST-C cup. Researchers will track their progress for up to five years using a standard hip score that measures pain, movement, and daily function.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Two types of hip replacement cup devices (Delta TT and Delta ST-C) used with the MINIMA stem
- What this could lead to
- If successful, this could help surgeons choose the better cup design for hip replacement, improving long-term mobility and pain relief for patients with hip arthritis.
- What could go wrong
- This is a relatively small study, and results may not apply to all patients. As with any surgery, there are risks like infection, implant loosening, or complications that could affect outcomes.
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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120 people
The number who actually took part.
- Started
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Feb 2022
- Expected to finish
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Feb 2029
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.
- 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: * Both genders * Any race * A diagnosis in the target hip of one or more of the following: a) non-inflammatory degenerative joint disease such as osteoarthritis, avascular necrosis; b) rheumatoid arthritis; c) post-traumatic arthritis; d) fractures of femoral neck; * patien willingness to partecipate and signature of informed consent form Exclusion Criteria: * local or systemic infection * septicaemia * persistent acute or chronic osteomyelitis * confirmed nerve or muscle lesion compromising hip joint function * vascular or nerve disease affecting the concerned limb * poor bone stock (for example due to osteoporosis) compromising the stability of the implant * metabolic disorders which may impair fixation and stability of the implant * any concomitant disease and dependence that might affect the implanted prosthsis * metal hypersensitivity to implant materials * required revision of previous standard femoral stem * women of childbearing potential who are pregnant, nursing, or planning to become pregnant, and those who do not agree to remail on an acceptable method of birth control throughout the entire study period * life expectancy less than 5 years
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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
-
The Orthopedic Clinic University Hospital Martin
Martin, 036 59, Slovakia
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Other studies related to the condition(s) this trial covers.
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