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Effect of Remazolam on Hemodynamics During Hepatectomy

Effect of Remazolam on Hemodynamics During Hepatectomy Under General Anesthesia Combined With Thoracic Epidural Anesthesia

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06565715
Enrollment
70
Registered
2024-08-22
Start date
2024-08-23
Completion date
2024-11-08
Last updated
2025-03-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hemodynamic Instability

Brief summary

There is high incidence of hemodynamic instability in patients undergoing hepatectomy with low central venous pressure, especially in general anesthesia combined with epidural anesthesia. Remazolam, a new benzodiazepine, has no significant cardiovascular inhibitory effect. Investigators hypothesis that remazolam will provide better hemodynamic when compared with propofol in patients undergoing hepatectomy with general anesthesia combined with epidural anesthesia.

Detailed description

Investigators plan to adopt the following strategies in the clinical study of this project: (1) To compare remazolam and propofol during anesthetic induction and maintenance; (2) Remazolam group: remazolam is administered 0.3mg/kg intravenous for anesthesia induction. Propofol group: propofol is administered 2mg/kg intravenous for anesthesia induction; (3) Epidural analgesia is used during perioperative period, and remifentanil pump injection is used during the operation to assist the subjects to tolerate the tracheal catheter; (4) the haemodynamic instability score (Hemodynamic instability score) is used to comprehensively evaluate intraoperative hemodynamic status. (5) To evaluate the incidence of postoperative complications. Through the above strategies, investigators further determine the optimization effect of remazolam, a novel benzodiazepine drug, on intraoperative hemodynamics in patients undergoing low central venous pressure hepatectomy, and further lay an empirical foundation for the routine use of remazolam in clinical hepatectomy.

Interventions

DRUGRemimazolam

Remimazolam is used for sedation during anesthetic induction and maintenance.

DRUGPropofol

propofol is used for sedation during anesthetic induction and maintenance.

Sponsors

Jun Zhang
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Patients who sign informed consent and are willing to complete the study according to the plan; 2. Over 18 years of age; 3. ASA grade Ⅰ \ Ⅲ; 4. Elective surgery; 5. General anesthesia combined with epidural anesthesia; 6. Child Pugh is classified as Level A

Exclusion criteria

1. Abnormal coagulation function; 2. Abnormal platelet; 3. A history of drug dependence; 4. Neurological diseases; 5. Severe sinus bradycardia (HR\<50 beats/min); 6. Atrial fibrillation; 7. Systolic blood pressure ≥200mmHg and/or diastolic blood pressure ≥120mmHg. 8. Cardiac insufficiency. 9. Child Pugh is classified as B or C.

Design outcomes

Primary

MeasureTime frameDescription
Hemodynamic instability scoreintraoperativeThe hemodynamic instability score is calculated as a weighted continuous measure ranging from 0 to 160 points, intended to reflect deviations of blood pressure and heart rate from predefined thresholds, and infusion rates of vasoactive agents and fluids.

Secondary

MeasureTime frameDescription
Cardiac index (CI)intraoperativeThe parameter of CI is measured by advanced hemodynamic monitoring device.
Stroke volume variation (SVV)intraoperativeThe parameter of SVV is measured by advanced hemodynamic monitoring device.
Systemic vascular resistance index (SVRI)intraoperativeThe parameter of SVRI is measured by advanced hemodynamic monitoring device.
Complications in 1 week after surgery1 week after surgeryComplications occured within 1 week after surgery

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026