Heart drug could replace morphine in gallbladder surgery recovery
NCT ID NCT07019818
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests whether a heart medication called esmolol can replace the morphine-like drug sufentanil during gallbladder surgery to improve recovery. About 120 adults having outpatient gallbladder surgery will receive either esmolol or sufentanil. The goal is to see if esmolol provides similar pain control and comfort with fewer side effects like nausea and vomiting.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Esmolol (a heart-specific beta-blocker) and Sufentanil (a morphine-like painkiller)
- What this could lead to
- If esmolol works as well as sufentanil, it could offer a way to manage pain during surgery without morphine-related side effects like nausea and vomiting.
- What could go wrong
- This is a small, early-phase study with only 120 participants. Esmolol may not control pain as effectively, and it can cause low blood pressure or breathing problems.
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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Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
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About 120 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Oct 2025
- Expected to finish
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Jan 2028
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: * Adult patients * ASA I to III * Scheduled outpatient cholecystectomy * General anesthesia with orotracheal intubation * Patient with signed consent * Patient affiliated to a social security scheme Exclusion Criteria: * Patients on beta-blockers * Uncontrolled hypertension * Contraindication to beta-blockers * Hypersensitivity to the active substance or to one of the excipients of sufentanil and esmolol * Pre-existing hemodynamic abnormality * Intubation planned to be difficult during the anaesthesia consultation * Severe obesity (BMI \> 35 kg/m2) * Pregnant or breast-feeding women * Patients deprived of liberty * Patients under guardianship
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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
2 sites. 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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CH Brive
RECRUITINGBrive-la-Gaillarde, France, 19100, France
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CHU Limoges
RECRUITINGLimoges, France, 87042, France
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