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Efficacy and safety of ciprofol vs etomidate for induction of general anesthesia in Off-pump coronary artery bypass grafting: a randomized, double-blind, clinical trial

Efficacy and safety of ciprofol vs etomidate for induction of general anesthesia in Off-pump coronary artery bypass grafting: a randomized, double-blind, clinical trial

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300068523
Enrollment
Unknown
Registered
2023-02-22
Start date
2022-11-18
Completion date
Unknown
Last updated
2023-05-22

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

Conditions

coronary artery disease

Interventions

Group A:ciprofol 0.2 mg/kg
Group B:ciprofol 0.3 mg/kg
Group C:etomidate 0.2 mg/kg

Sponsors

General Hospital of Northern Theater Command
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Above 18 years old; 2. ASA score ?-?; 3. BMI 18-30 kg/m2; 4. Patients who plan to undergo elective off-cardiopulmonary bypass grafting.

Exclusion criteria

Exclusion criteria: 1. NYHA cardiac function class IV, or patients with left ventricular ejection fraction (LVEF) < 40%; 2. Patients with preoperative hemodynamic instability, emergency surgery and secondary surgery; 3. Patients with difficult airway, modified Mallampati grade IV patients; 4. Hepatic and renal insufficiency; 5. Nervous or mental disorders, epilepsy; 6. Those who are known to be allergic to active ingredients or excipients of cyclopofol or propofol injection; 7. Drug or alcohol abuse; 8. Patients who are pregnant or breastfeeding; patients who plan to become pregnant within 1 month after surgery; 9. In addition to the primary disease, patients with obvious abnormal results of preoperative physical examination or laboratory examination; 10. Patients who refuse to participate.

Design outcomes

Primary

MeasureTime frame
the area under the curve below baseline MAP (MAP-time integral);

Secondary

MeasureTime frame
change of CI and SVV;The maximum decrease in MAP;Minimum mean arterial pressure, MAPmin;Heart rate variation;change of BIS value;Incidence of adverse reactions;Anesthesiologists' satisfaction;the use of vasopressors;

Countries

China

Contacts

Public ContactYugang Diao

General Hospital of Northern Theater Command

Diao72@163.com+86 153 0988 1160

Outcome results

None listed

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