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Comparison of the efficacy and safety of ciprofol versus propofol for rapid sequence intubation induction: a randomized, non-inferiority trial

Comparison of the efficacy and safety of ciprofol versus propofol for rapid sequence intubation induction: a randomized, non-inferiority trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500095742
Enrollment
Unknown
Registered
2025-01-13
Start date
2025-10-21
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Patients undergoing elective non cardiac surgery under general anesthesia and tracheal intubation

Interventions

propofol group (group P) :During rapid sequence induction and intubation, patients receive propofol (2.0 mg/kg) as the induction agent.
ciprofol group (group C):During rapid sequence induction and intubation, patients receive ciprofol (0.4 mg/kg) as the induction agent.

Sponsors

Zhongshan Hospital (Xiamen), Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients undergoing elective non cardiac surgery; 2. Tracheal intubation is required for general anesthesia induction; 3. Gender is not limited, age range is 18 to 65 years old; 4. American College of Physicians (ASA) grades I-III; 5. Mallampati airway rating is I-II grade; 6. Voluntary participation, signed informed consent form.

Exclusion criteria

Exclusion criteria: 1. Those who have respiratory infectious diseases or use hormone or bronchodilator within 2 weeks; 2. Patients predicted to have difficult airways; 3. BMI>=35kg/m^2; 4. Individuals with mental illnesses who are unable to cooperate; 5. History of allergies to opioid drugs, propofol, or cyclosporine components (i.e. soybean oil, glycerol, triglycerides, egg yolk lecithin, sodium oleate, and sodium hydroxide).

Design outcomes

Primary

MeasureTime frame
Intubation conditions;

Secondary

MeasureTime frame
The incidence of induced hypotension;Changes in heart rate during induction;Success rate of general anesthesia induction;Time for successful induction of general anesthesia;Incidence of injection pain;Mean BIS value during induction;Study the use of medication supplementation doses and/or remedial drugs.;

Countries

China

Contacts

Public ContactLin Yimei

Zhongshan Hospital (Xiamen), Fudan University

lin.yimei@zsxmhospital.com+86 183 5918 5906

Outcome results

None listed

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