No-Opioid anesthesia beats standard for gallbladder surgery recovery
NCT ID NCT07307625
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested whether avoiding opioids during gallbladder surgery could improve recovery. 101 patients received either opioid-free anesthesia (using lidocaine and dexmedetomidine) or standard opioid anesthesia. The opioid-free group had less pain after surgery, needed fewer painkillers, and had less nausea and vomiting. They also woke up faster and had better early recovery scores.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- lidocaine and dexmedetomidine
- What this could lead to
- If confirmed, this approach could offer a safer, more comfortable anesthesia option for gallbladder surgery, reducing opioid use and side effects like nausea.
- What could go wrong
- This was a small, single-center trial with only 101 patients. Larger, more diverse studies are needed to confirm these results and ensure safety for broader use.
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
-
101 people
The number who actually took part.
- Started
-
Dec 2024
- Finished
-
Dec 2025
- Lead sponsor
-
A government agency
The lead sponsor is a government body.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 to 65 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 18-65 * ASA I-II * Elective laparoscopic cholecystectomy * Informed consent * BMI 18-30 kg/m² * Normal liver and renal function Exclusion Criteria: * Refusal to participate * Allergy to study drugs * Chronic opioid use * Major organ disease * Pregnancy or lactation * Open surgery conversion * Recent participation in another trial
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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
-
SBÜ Kartal Dr. Lütfi Kırdar City Hospital
Istanbul, Turkey (Türkiye)
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Other studies related to the condition(s) this trial covers.
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