Can a diabetes drug improve joint replacement outcomes?
NCT ID NCT07755085
First seen Aug 10, 2026 · Last updated Aug 11, 2026 · Updated 1 time
Summary
This trial tests whether taking a GLP-1 medication (semaglutide) for at least six months before hip or knee replacement surgery can improve recovery and reduce complications in patients with obesity. Participants will be randomly assigned to receive either the medication plus behavioral support (diet, exercise, counseling) or a placebo with the same support. The study will track wound complications, weight loss, and mobility changes to see if this approach helps high-risk patients.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- semaglutide (a GLP-1 receptor agonist) combined with structured behavioral modification (diet, exercise, counseling)
- What this could lead to
- If effective, this approach could reduce surgical complications and improve recovery for obese patients undergoing joint replacement, potentially leading to better standard care.
- What could go wrong
- This is a small pilot study, so results may not be conclusive. The medication may not reduce complications and could have side effects, and the behavioral program adds complexity.
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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Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
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About 100 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Oct 2026
An estimate. Start dates often move.
- Expected to finish
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Dec 2028
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.
- Ages
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18 to 90 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 Criteria: * Patients with a diagnosis of hip or knee arthritis and are a deemed candidate for THA or TKA by an orthopaedic surgeon * Diagnosis of BMI 35+ with an obesity-related health condition (Coronary vascular disease, previous stroke, type 2 diabetes, hypertension, dyslipidemia, obstructive sleep apnea, asthma) or BMI 40+ * Patients must be between 18-90 years of age * Able to provide informed consent Exclusion Criteria: * Cognitive impairment that precludes study participation and compliance * Patients unwilling to undergo smoking cessation prior to surgery * Patients currently taking biologic medications that suppress the immune system * Patients currently taking GLP-1 medications * Patients with a contraindication to GLP-1 medication
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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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Nova Scotia Health
Dartmouth, Nova Scotia, B2Y 2N5, Canada
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