Nerve block showdown: which injection eases gallbladder surgery pain best?
NCT ID NCT07661693
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study compares two types of nerve blocks—erector spinae plane block and subcostal transversus abdominis plane block—for pain after laparoscopic gallbladder removal. One hundred adults having elective surgery will receive one of the two blocks, and researchers will track how much opioid pain medicine they need in the first 24 hours. The goal is to see which block provides better pain control and fewer side effects.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- nerve block (local anesthetic injection)
- What this could lead to
- If one block proves better, it could reduce opioid use and improve recovery for people having gallbladder surgery.
- What could go wrong
- This is a small, early-stage comparison. Results may not apply to other surgeries or patients with different health conditions.
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 100 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jun 2027
An estimate. Start dates often move.
- Expected to finish
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Sep 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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Children (under 18), adults (18 to 64) and older adults (65 and over)
- 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: Adults aged 18 years and older Scheduled for elective laparoscopic cholecystectomy under general anesthesia American Society of Anesthesiologists (ASA) physical status I-III Ability to understand the study protocol and provide written informed consent - Exclusion Criteria:Refusal to participate Known allergy or contraindication to local anesthetic agents Coagulopathy or anticoagulant therapy contraindicating regional anesthesia Infection at the planned injection site Body mass index (BMI) \> 35 kg/m² Chronic opioid use or opioid dependence Chronic pain syndromes requiring regular analgesic treatment Severe hepatic, renal, or cardiac dysfunction Pregnancy or breastfeeding Inability to communicate or assess pain using the Numerical Rating Scale (NRS) \-
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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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Gaziantep City Hospital
Şahinbey, Gaziantep, 27060, Turkey (Türkiye)