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A comparative study on the postoperative recovery quality of patients under general anesthesia using remimazolam and propofol based on the QoR-15 score

A comparative study on the postoperative recovery quality of patients under general anesthesia using remimazolam and propofol based on the QoR-15 score

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500114063
Enrollment
Unknown
Registered
2025-12-08
Start date
2025-12-08
Completion date
Unknown
Last updated
2025-12-15

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

Conditions

Postoperative recovery quality

Interventions

Sponsors

Women’s Hospital, Zhejiang University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1.Female patients scheduled for laparoscopic surgery under elective intravenous general anesthesia; 2.age 18-60y; 3.ASA ?~?; 4.BMI 18-24 kg/m2;

Exclusion criteria

Exclusion criteria: 1.The use of sedatives, antidepressants or other drugs that affect electroencephalogram (EEG) monitoring recently or before anesthesia induction; 2.with abnormal neurological function; 3.with severe abnormalities in heart, lung, liver and kidney functions; 4.Patients with cardiovascular diseases such as hypertension or those taking drugs that affect the cardiovascular system; 5.Diabetics; 6.history of alcohol abuse and drug abuse; 7.Known to be allergic to the research drug; 8.Those who refuse to sign the informed consent form;

Design outcomes

Primary

MeasureTime frame
Postoperative recovery quality;

Secondary

MeasureTime frame
Time of loss of consciousness;Time of Extubation;The incidence of hypotension after induction;The incidence of perioperative adverse events;Intraoperative hemodynamic changes;

Countries

China

Contacts

Public ContactLihong Sun

Women’s Hospital, Zhejiang University School of Medicine

sunlh1201@163.cm+86 571 87061501

Outcome results

None listed

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