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Comparison of the effects of Ciprofol and Propofol induction on hemodynamics during the anesthesia Induction period in patients undergoing liver transplantation

Comparison of the effects of Ciprofol and Propofol induction on hemodynamics during the anesthesia Induction period in patients undergoing liver transplantation

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500104905
Enrollment
Unknown
Registered
2025-06-25
Start date
2025-07-01
Completion date
Unknown
Last updated
2025-06-30

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

Conditions

End-stage liver disease

Interventions

Group P (Propofol Group):anesthesia induction with propofol
Group C (Ciprofol Group):anesthesia induction with ciprofol

Sponsors

The First Affiliated Hospital,Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.Patients scheduled for liver transplantation in this hospital. 2.ASA classification Grade I - IV; 3.Aged 18-65 years, regardless of gender; 4.Able to communicate effectively and willing to participate in this study;

Exclusion criteria

Exclusion criteria: 1.Untreated stage 2 and stage 3 hypertension; 2.Known allergies to eggs, soy products, propofol, or ciprofol; 3.Other reasons that make the investigator believe the patient is not suitable for inclusion in the clinical trial;

Design outcomes

Primary

MeasureTime frame
The dosage of norepinephrine used during the anesthesia induction period.;

Secondary

MeasureTime frame
The average degree of fluctuation of systemic vascular resistance index during the anesthesia induction period.;The fluctuation of mean arterial pressure during the anesthesia induction period.;The maximum decrease in mean arterial pressure.;The average degree of fluctuation of the cardiac index during the anesthesia induction period.;Blood lactic acid levels during the anesthesia induction period;

Countries

China

Contacts

Public ContactYang lu

The First Affiliated Hospital,Sun Yat-sen University

yanglu6@mail.sysu.edu.cn+86 139 2950 8567

Outcome results

None listed

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