New pain block could cut opioid use after gallbladder surgery
NCT ID NCT06123117
First seen Jun 26, 2026 · Last updated Jun 26, 2026 · Updated 1 time
Summary
This study compares two ways to manage pain after laparoscopic gallbladder removal. One group gets standard local anesthesia at the incision sites, while the other also receives a nerve block guided by the surgery camera. The goal is to see if the added block reduces pain and the need for opioid painkillers. About 850 adults having gallbladder surgery will take part.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- ropivacaine
- What this could lead to
- If it works, this could provide a better way to manage pain after gallbladder surgery, reducing the need for strong painkillers.
- What could go wrong
- This is an early-stage trial testing a procedure, not a new drug. Previous smaller studies have not shown a clear benefit for the added nerve block, so results may not be conclusive.
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 850 people
The number the study aims to enrol. It can still change while the study runs.
- Started
-
Jan 2024
- Expected to finish
-
Oct 2027
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.
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: * All patients scheduled for elective or emergency LCC, aged over 18 and able to give an informed consent. Exclusion Criteria: * Age under 18 years, chronic daily opioid and/or pain tolerance / pain threshold -modifying medication use (abuse), pregnancy, known allergy to local anesthetics, diagnosed severe coagulopathy and incapability to give informed consent for whatever reason.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Cholecystitis are added.
Genom att skicka in godkänner du våra Användarvillkor
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.
-
The places running it
1 site. The list below names each one and where it is.
-
The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
-
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
-
Jorvi hospital / HUS
RECRUITINGEspoo, Uusimaa, 00029, Finland
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can a simple score spot hidden gallbladder cancer?
- Robot could remove gallbladder and clear bile duct stones in one operation
- Can a homemade bag make gallbladder surgery safer?
- Can an immunotherapy combo turn inoperable gallbladder cancer into a surgical success?
- Can a simple anesthetic choice prevent Post-Surgery vomiting?
- Can a new infrared camera help surgeons spot nerves and bile ducts?