A new anesthesia drug may keep blood pressure steadier during liver surgery
NCT ID NCT07789275
First seen Aug 27, 2026 · Last updated Aug 28, 2026 · Updated 1 time
Summary
This trial tests whether remimazolam, an intravenous anesthetic, prevents low blood pressure better than propofol during major liver surgery. Adults having at least three liver segments removed will receive one of the two drugs to maintain anesthesia. Researchers will measure how low blood pressure drops and how long it stays low, and they will also track bleeding, transfusions, recovery, and complications. The goal is to see if remimazolam offers a safer anesthesia option for this high-risk surgery.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- remimazolam
- What this could lead to
- If remimazolam works, it could offer a safer anesthesia option for major liver surgery, reducing the risk of low blood pressure and its complications.
- What could go wrong
- This is a single-center trial, and results may not apply to all patients. Remimazolam may not outperform propofol, and any anesthesia carries risks.
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 224 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Aug 2026
An estimate. Start dates often move.
- Expected to finish
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Aug 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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18 to 85 years
- 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: * Age 18 to 85 years * Scheduled for elective liver resection * Preoperative surgical plan includes resection of at least three Couinaud liver segments * Planned use of low central venous pressure management, general anesthesia, invasive arterial pressure monitoring, and central venous pressure monitoring * American Society of Anesthesiologists physical status II or III * Both study anesthesia strategies are considered clinically appropriate * Able to understand the study information and provide written informed consent Exclusion Criteria: * Emergency surgery or inability to complete written informed consent before surgery * Known contraindication or serious hypersensitivity to remimazolam, another benzodiazepine, propofol, or a relevant excipient * Preoperative shock, ongoing vasoactive drug support, or another hemodynamically unstable condition that makes either study anesthesia strategy unsafe * Child-Pugh class C, Model for End-Stage Liver Disease score of 20 or higher, or end-stage liver disease in the investigator's judgment * Massive ascites, recent variceal bleeding, clinically important hypersplenism with severe thrombocytopenia, or portal hypertension sufficient to substantially alter circulatory management * Regular long-term benzodiazepine use, drug dependence, or alcohol misuse expected to affect the pharmacological evaluation * Clinical requirement for an inhalational anesthetic or another maintenance anesthesia strategy incompatible with randomized assignment * Pregnant or breastfeeding * Concurrent participation in another interventional study that may affect the primary outcome * Any other condition that, in the investigator's judgment, makes participation unsafe or prevents completion of the study procedures
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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
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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Beijing Tsinghua Changgung Hospital
Beijing, Beijing Municipality, 102218, China
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