New study aims to cut opioid use after joint replacement
NCT ID NCT06230081
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether adding ultrasound-guided nerve blocks before hip or knee replacement surgery can reduce pain and opioid use compared to standard pain management. 400 adults with osteoarthritis will be enrolled. The goal is to improve recovery and reduce side effects like nausea.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Ropivacaine and clonidine (local anesthetic and pain reliever)
- What this could lead to
- If successful, this could lead to better pain control and faster recovery after joint replacement, with less reliance on opioids.
- What could go wrong
- This is a single study with 400 participants, and results may not apply to all patients. Nerve blocks carry small risks like infection or nerve damage.
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
-
About 400 people
The number the study aims to enrol. It can still change while the study runs.
- Started
-
Feb 2024
- Expected to finish
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Apr 2026
An estimate. End dates often move.
- 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
-
18 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: * Osteoarthritis of the knee- or hip necessitating total knee- or hip replacement * Patients who understand the conditions of the study and are willing to participate for the length of the prescribed follow-up Exclusion Criteria: * Known allergy to local anesthetics or other contraindication for the use of local anesthetics. * Coagulopathy * Bilateral operation * Revision arthroplasty
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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
-
Dept of Anaesthesiology, Trelleborg Hospital
Trelleborg, Sweden
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Other studies related to the condition(s) this trial covers.
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