Gut bugs may decide if your new knee lasts
NCT ID NCT06951477
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This study looks at whether the bacteria in your gut (the gut microbiome) is different in people whose knee replacements fail versus those whose knees work well. Researchers will compare gut bacteria in 30 patients needing repeat knee surgery to those with successful implants. They hope to understand if gut health plays a role in infection, loosening, or pain after knee replacement.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could point toward ways to predict or prevent knee replacement failure by targeting the gut microbiome.
- What could go wrong
- This is a small, early observational study with only 30 participants, so results may not apply to everyone. It looks for patterns, not a treatment.
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 30 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Oct 2025
An estimate. Start dates often move.
- Expected to finish
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Dec 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
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 at University Hospital scheduled to undergo a revision TKA.
- Ages
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Children (under 18), adults (18 to 64) and older adults (65 and over)
- 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: * Scheduled to undergo a revision TKA * Willing and able to comply with follow-up requirements * Ability to provide informed consent * Ability to read, write, and speak English Exclusion Criteria: * Pregnancy * Less than 3 months post-operation from primary surgery * Diagnosis of periprosthetic fracture * Scheduled for DAIR (debridement, antibiotics, and implant retention) revision surgery * Scheduled for stage 2 PJI revision
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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University Hospital
London, Ontario, N6A5A5, Canada
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