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Clinical Trials in China / NCT07116733
Recruiting Phase 3

Desflurane vs. Propofol for Cardiac Anesthesia

NCT07116733 · tracked via the Priya Life Science China tracker
Sponsor
Xijing Hospital
Phase
Phase 3
Started
2025-10-20
Last updated
2025-11-25

Condition(s) studied

Cardiac SurgeryCoronary Artery Bypass Grafting

Investigational drug(s) / intervention(s)

Desflurane groupPropofol group

Desflurane group: After routine induction, maintain anesthesia with inhaled desflurane , adjusting concentration as needed to sustain 0.5-2 MAC . To maximize the cardioprotective effects of inhaled anesthetics, adhere to this intraoperative strategy: Maintain ≥1 MAC continuous desflurane for ≥30 minutes ; For on-pump CABG , discontinue desflurane 15 minutes before initiating cardiopulmonary bypass (CPB) ; If intraoperative desflurane cessation is required, implement a wash-in/wash-out strategy (recommended but non-mandatory): Perform 3 alternating cycles of: Wash-in : ≥10 minutes of desflurane at ≥0.5 MAC, Wash-out : ≥10 minutes of complete cessation of inhaled anesthetics. Propofol is strictly prohibited for anesthesia maintenance throughout the procedure , except during CPB.

Propofol group: Administer total intravenous anesthesia (TIVA) using propofol infusion at 3-8 mg/kg/h . No inhaled anesthetics are permitted for maintenance. This may be delivered via:target-controlled infusion (TCI) systems, or manual adjustment of intravenous infusion rates.

Study summary

To investigate whether the inhaled anesthetic desflurane, compared with propofol, exerts cardioprotective effects and reduces the incidence of severe postoperative major cardiac events in patients undergoing coronary artery bypass graft (CABG) surgery.

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
Inclusion Criteria: 1. Patients scheduled for elective coronary artery bypass grafting (CABG) 2. Age ≥ 18 years old; 3. Sign the informed consent form. Exclusion Criteria: 1. Emergency or urgent operation 2. Concomitant valve or aortic surgery 3. History of myocardial infarction in recent 30 days 4. Current use of myocardial preconditioning-affecting medications, such as sulfonylurea (glibenclamide), allopurinol, theophylline, nicorandil(last dose \< 8 hrs), etc 5. Participated in other randomized controlled clinical trials in recent 3 months 6. General anesthesia in recent 30 days 7. History of kidney and liver transplantation, or severe liver and kidney dysfunction (EGFR ≤ 20 mlgmin/1.73 m2, conventional dialysis or patients who have started dialysis; Child Pugh grade C/cirrhosis) 8. History of open heart surgery; 9. Hemodynamic instability or severe heart failure (SBP\<90 mmHg or preoperative need of high-dose vasoactive drug support, placement of aortic balloon pump (IABP), ECMO or ventricular assist device, left ventricular ejection fraction\<30%) 10. Adverse drug reactions to trial medications 11. History of malignant hyperthermia 12. Pregnancy or lactation

Primary outcome measure(s)

Trial sites (14)

FacilityCityRegionStatus
Fuzhou University Affiliated Provincial Hospital Fuzhou Fujian Not Yet Recruiting
Cangzhou People's Hospital Cangzhou Hebei Not Yet Recruiting
Hebei General Hospital Shijiazhuang Hebei Not Yet Recruiting
The First Hospital of Hebei Medical University Shijiazhuang Hebei Not Yet Recruiting
The First Affiliated Hospital of Zhengzhou University Zhengzhou Henan Not Yet Recruiting
Wuhan Asia Heart Hospital Wuhan Hubei Not Yet Recruiting
Jiangsu Province Hospital Nanjin Jiangsu Not Yet Recruiting
Xijing Hospital Xi'an Shaanxi Recruiting
Sichuan Provincial People's Hospital Chengdu Sichuan Not Yet Recruiting
Tianjin Chest Hospital Tianjin Tianjin Municipality Recruiting
Ningbo No.2 Hospital Ningbo Zhejiang Not Yet Recruiting
Daping Hospital, Army Medical University Chongqing China Not Yet Recruiting
Changhai Hospital Shanghai China Recruiting
Zhongshan Hospital, Fudan University Shanghai China Not Yet Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07116733 on ClinicalTrials.gov ↗ ← All trials in China