A shot at smoother recovery: knee replacement pain blocks put to the test
NCT ID NCT07751653
First seen Aug 07, 2026 · Last updated Sep 15, 2026 · Updated 2 times
Summary
This trial compares three common anesthetic blocks used during knee replacement surgery to see which one controls pain best right after the operation. It also looks at how well patients can move their knee in the first few days, and whether pain and recovery differ by age or sex. The goal is to find the most effective approach for easing discomfort and speeding up early recovery.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Levobupivacaine plus mepivacaine (a local anesthetic combination) injected as a single shot at the end of surgery
- What this could lead to
- If one block proves better, it could become the standard choice for knee replacement, helping patients recover with less pain and better movement.
- What could go wrong
- This is a single trial with 141 participants, so results may not apply to everyone. Blocks can cause temporary weakness or other complications.
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
-
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
-
141 people
The number who actually took part.
- Started
-
Feb 2025
- Finished
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May 2026
- Lead sponsor
-
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
-
40 years and older
- Sex
-
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: * Total Knee prosthesis * ASAC I-II * signed Informed consent form Exclusion Criteria: * \<40 years * Mental confusion and delirium * Coagulation disorders
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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
-
Ospedale Galeazzi S.p.A.
Milan, Italy, 20100, Italy
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