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Comparison of ciprofol versus propofol for delayed extubation after major noncardiac surgery: a retrospective cohort study

Comparison of ciprofol versus propofol for delayed extubation after major noncardiac surgery: a retrospective cohort study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400092539
Enrollment
Unknown
Registered
2024-11-19
Start date
2024-12-01
Completion date
Unknown
Last updated
2024-12-02

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

Conditions

None

Interventions

Sponsors

Nanfang Hospital, Southern Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Patients undergoing elective non-cardiac surgery under general anesthesia; 2.Adult (>18 years old) patients admitted to the PACU for anesthesia awakening after surgery; 3.Propofol or ciprofol was used for induction and maintenance of general anesthesia;

Exclusion criteria

Exclusion criteria: 1.ASA Physical Status Classification V and VI; 2.Simultaneous or alternating use of ciprofol and propofol during surgery; 3.Intraoperative laryngeal mask ventilation; 4.Operation time <= 30 minutes; 5.Patients with preoperative chronic renal failure (patients requiring renal replacement therapy or who have undergone renal transplantation); 6.Data with logical errors that are difficult to verify;

Design outcomes

Primary

MeasureTime frame
PACU extubation delay rate (>1h);Time to extubation;

Secondary

MeasureTime frame
PACU stay time;

Countries

China

Contacts

Public ContactLiu Kexuan

Nanfang Hospital, Southern Medical University

liukexuan705@163.com+86 20 61641888

Outcome results

None listed

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