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A comparative study of the effect of propofol and remimazolam on blood pressure during general anesthesia

Effect of general anesthetics propofol and remimazolam on mean circulatory filling pressure: A randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT1011210026
Enrollment
60
Registered
2021-07-30
Start date
2021-07-30
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

pancreatic cancer, hepatic cancer, bladder cancer, colon cancer, gastric cancer pancreatic cancer, hepatic cancer, bladder cancer, colon cancer, gastric cancer

Interventions

The patients will be randomly assigned to two groups: remimazolam and propofol. Random assignment will be performed using Mujinwari (URL: https://mujinwari.biz/users/login). Age, sex, BMI, and presenc
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mean circulatory filling pressure propofol remimazolam

Sponsors

Tomohiro Chaki
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Patients scheduled to undergo standby surgery under general anesthesia in the operating room of Sapporo Medical University Hospital. (2) Patients scheduled to undergo open pancreaticoduodenectomy or liver resection surgery. (3) The patient is scheduled to undergo arterial pressure monitoring using an arterial line under general anesthesia. (4) Adults aged 20 years or older at the time of surgery. (5) The patient's preoperative condition should be ASA-PS (American Society of Anesthesiologists Physical Status) 1-2 and in good general condition.

Exclusion criteria

Exclusion criteria: (1) Patients with contraindications to propofol or remimazolam (2) Patients who are allergic to propofol, remimazolam, midazolam, or flumazenil. (3) Patients who are allergic to propofol, remimazolam, midazolam, or flumazenil. (4) Patients with severe hepatic or renal dysfunction that may affect drug metabolism. (5) Patients with severe hepatic or renal dysfunction that may affect drug metabolism (5) Other patients who are judged inappropriate for participation in this study by the principal investigators and sub-investigators

Design outcomes

Primary

MeasureTime frame
Changes in mean circulatory filling pressure before and after induction of general anesthesia and 30 minutes after induction of general anesthesia

Secondary

MeasureTime frame
Patient background (age, gender, body weight, ASA PS, underlying diseases including hypertension, and presence of antihypertensive medication) Changes in heart rate (HR) before and 30 minutes after induction of general anesthesia Change in body blood pressure (NBP) before and 30 minutes after induction of general anesthesia Transcutaneous arterial blood oxygen saturation (SpO2) Changes in perfusion index (PI) before and 30 minutes after induction of general anesthesia Change in the single cardiac output coefficient (esSVI) before and 30 minutes after induction of general anesthesia Cardiac coefficient (esCCI) before and 30 minutes after induction of general anesthesia Depth of anesthesia bispectral index (BIS) at each measurement time point Total dose of remimazolam and propofol during induction of anesthesia Incidence of adverse events: severe hypotension, use of hypertensive drugs, bradycardia, cardiac arrest

Contacts

Public ContactChaki Tomohiro

Sapporo Medical University

chakitomohiro0728@yahoo.co.jp+81-116889663

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026