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Effect of rimazolam versus propofol on the quality of recovery in patients undergoing laparoscopic cholecystectomy

Effect of rimazolam versus propofol on the quality of recovery in patients undergoing laparoscopic cholecystectomy: a randomized controlled trial

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300078641
Enrollment
Unknown
Registered
2023-12-14
Start date
2024-01-01
Completion date
Unknown
Last updated
2023-12-19

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

Conditions

laparoscopic cholecystectomy

Interventions

Rimazolam group :Induction and maintenance of anesthesia by intravenous administration of rimazolam
Propofol group:Induction and maintenance of anesthesia by intravenous administration of propofol

Sponsors

The First Affiliated Hospital of Shantou University Medical College
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1) Age 18-65 years old 2) BMI 18-28 kg/m2 3) ASA classification of I-III 4) voluntary participation in the study, and informed consent signed

Exclusion criteria

Exclusion criteria: 1) History of allergy to benzodiazepines, opioids or propofol 2) Significant abnormalities in blood routine or blood biochemical indicators 3)Diagnosed as serious systemic diseases such as circulatory, respiratory, hematological, hepatic and renal diseases or poorly controlled diabetes 4)Neurological, psychiatric or communication disorders that prevent cooperation 5) Pregnant or breastfeeding women and those who have a birth-plan within 3 months 6) Patients who have difficulty maintaining normal intraoperative vital signs or who have serious complications and need to be transferred to the ICU 7)Patients who have participated in other clinical trial within the last 3 months

Design outcomes

Primary

MeasureTime frame
QoR-15 scale scores ;

Secondary

MeasureTime frame
Total use of narcotics and vasoactive drugs;Intraoperative vital signs ;Adverse events during anesthesia recovery period;

Countries

China

Contacts

Public ContactSun Wei

The First Affiliated Hospital of Shantou University Medical College

md.sunwei@gmail.com+86 135 8057 9456

Outcome results

None listed

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