Nerve block may ease pain after carpal tunnel release
NCT ID NCT05372393
First seen Jun 24, 2026 · Last updated Jun 26, 2026 · Updated 1 time
Summary
This study tests whether adding a nerve block to local anesthesia reduces pain after carpal tunnel release surgery. 118 adults with carpal tunnel syndrome will be randomly assigned to receive either local anesthesia alone or local anesthesia plus a nerve block. Pain levels will be tracked for 72 hours after surgery.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- local infiltration anaesthesia (lidocaine, bupivacaine, sodium bicarbonate) with or without distal median nerve block
- What this could lead to
- If adding a nerve block works, it could mean less pain after carpal tunnel surgery without needing stronger anesthesia.
- What could go wrong
- This is a small, early-stage trial (118 people) comparing two anesthesia methods. The nerve block may not reduce pain enough to be worth the extra step.
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 118 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Sep 2022
- Expected to finish
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Apr 2026
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 years and older
- 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: * ≥18 years of age * CTS verified by nerve conduction studies * Symptoms suitable for CTS Exclusion Criteria: * Recurrent CTS * Peripheral neuropathies * Known allergy to the trial drugs * Profound cognitive impairment * Pregnancy
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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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Kuopio University hospital, Department of Orthopaedics, Traumatology and Hand Surgery
RECRUITINGKuopio, Northern Savonia, 70210, Finland
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Other studies related to the condition(s) this trial covers.
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