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The Clinical Use of Remimazolam for General Anesthesia Induction and Maintenance in Day Surgery

The Clinical Use of Remimazolam for General Anesthesia Induction and Maintenance in Day Surgery

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400088335
Enrollment
Unknown
Registered
2024-08-15
Start date
2022-11-09
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

None listed

Interventions

Remimazolam group:During anesthesia induction, 0.2 mg/kg remimazolam was injected intravenously, followed by a constant intravenous pump at 0.5 mg/kg/h. During anesthesia maintenance, remazolam doses
Propofol group:During anesthesia induction, plasma target controlled infusion of propofol was 3µg/ml, and during anesthesia maintenance, the dose of propofol was maintained at 2-3µg/ml.

Sponsors

The First Affiliated Hospital of Guangxi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Patients scheduled for elective surgery at the Day Surgery Center of the First Affiliated Hospital of Guangxi Medical University from December 2021 to September 2022, with scheduled surgical duration of less than 2 hours, aged 18 to 65 years, ASA grade I to II, BMI 18 to 25 kg/m2, and Mallampati grade I to III were included

Exclusion criteria

Exclusion criteria: (1) Patients with other severe complications such as diabetes, severe obesity, chronic obstructive pulmonary disease, asthma, severe hypertension, etc.; (2) Mental disorders; (3) Hematological disorders such as anemia, thrombocytopenia, leukemia, etc.; (4) Hepatic dysfunction; (5) Substance abuse; (6) Alcoholism or allergy to drugs, especially to propofol and benzodiazepines; (7) Pregnant or lactating women; (8) Participation in any other drug clinical trials within the past 3 months; (9) Baseline blood pressure: systolic pressure 180 mmHg, diastolic pressure 100 mmHg.

Design outcomes

Primary

MeasureTime frame
Efficacy;Safety;

Secondary

MeasureTime frame
Mean arterial pressure (MAP);Heart rate (HR);the time to loss of consciousness (LOC);Incidence of injection pain;Number of patients requiring vasopressor support to maintain circulation during surgery;Time from cessation of medication to eye opening;Time from cessation of medication to extubation;PACU stay duration;Time to achieve MOAA/S score > 4 after cessation of medication;Visual Analog Scale (VAS) scores 30 minutes post-extubation;Occurrence of adverse reactions in patients during follow-up on the first and seventh postoperative days;

Countries

China

Contacts

Public ContactYunan Lin

The First Affiliated Hospital of Guangxi Medical University

277464077@qq.com+86 137 6827 8751

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026