Nerve block strategy tested to prevent chronic pain after knee replacement
NCT ID NCT06182059
First seen Sep 21, 2026 · Last updated Sep 21, 2026
Summary
Researchers compare two regional anesthesia approaches for people having total knee replacement. One approach uses a fast-track protocol, while the other uses continuous infusions through femoral and sciatic catheters. The trial measures whether the continuous catheter method reduces persistent pain six months after surgery, along with acute pain and morphine use in the first days after the operation.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- continuous peripheral nerve block
- What this could lead to
- If the fast-track nerve block protocol works, it could become a standard way to lower the chance of long-term pain after knee replacement.
- What could go wrong
- The trial may show no difference between the two anesthesia methods, or the results might not apply to all patients. Nerve blocks carry small risks like nerve irritation or infection.
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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About 436 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jan 2024
- Expected to finish
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Jul 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.
- Ages
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18 to 85 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: * primary total knee replacement with a written informed consent Exclusion Criteria: * Allergy to local anesthetics or any drugs involve in the study * Controindication to regional anesthesia * chronic use of opioids * BMI \> 35 kg m2
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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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Policlinico di Monza SPA
RECRUITINGMonza, Monza Brianza, 20900, Italy
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