New nerve block could cut opioid use for liver donors
NCT ID NCT07233096
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether a special nerve block, called a rectus-intercostal fascial plane block, can reduce pain and the need for morphine in people who donate part of their liver. Sixty-four donors were randomly assigned to receive either the nerve block plus standard painkillers or standard painkillers alone. The goal was to see if the block leads to less morphine use and better pain scores in the first 24 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
- bupivacaine (a numbing medicine) given as a nerve block
- What this could lead to
- If it works, this nerve block could become a standard way to reduce pain and the need for strong painkillers after liver donation surgery.
- What could go wrong
- This is a small, single-center study with only 64 participants. The block may not provide meaningful pain relief for everyone, and there is a small risk of side effects like bruising or infection at the injection site.
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
-
64 people
The number who actually took part.
- Started
-
Dec 2025
- Finished
-
Jun 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
-
18 to 75 years
- 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: * Age between 18 and 75 years * Patients with American Society of Anesthesiology (ASA) physical status I-II * Patients scheduled for a living donor hepatectomy Exclusion Criteria: * Allergy to local anesthetics * Coagulopathy * Skin infection at the block area * Advanced renal failure * Chronic pain syndromes * Alcohol or drug abuse * Psychiatric 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
-
istinye University
Istanbul, Turkey (Türkiye)
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Other studies related to the condition(s) this trial covers.
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