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Effects of propofol and sevoflurane on cerebral oxidative stress in patients undergoing hepatobiliary surgery

Effects of propofol and sevoflurane on cerebral oxidative stress in patients undergoing hepatobiliary surgery

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300069918
Enrollment
Unknown
Registered
2023-03-29
Start date
2023-04-01
Completion date
Unknown
Last updated
2023-09-04

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

Conditions

Anesthetic drug neurotoxicity

Interventions

Sevoflurane group:Maintenance of anesthesia with sevoflurane during operation
Propofol group:Maintenance of anesthesia with propofol during operation

Sponsors

Xuzhou Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1) 18 to 60 years 2) ASA grade?-? 3) Patients with indications for hepatobiliary surgery and operating time of not less than 2 hours 4) Agreed to participate in this study and signed an informed consent form

Exclusion criteria

Exclusion criteria: 1) Contraindications to the use of propofol or sevoflurane 2) Patients with severe heart, lung, kidney and other important organ diseases 3) Patients with severe infectious diseases, endocrine system diseases and blood system diseases 4) Those who have a history of smoking, alcohol and drug abuse 5) Received radiation and took antioxidants a week before operation

Design outcomes

Primary

MeasureTime frame
8-hydroxy-2 deoxyguanosine;

Secondary

MeasureTime frame
Protein carbonyl;8-iso-prostaglandin F2a;Superoxide dismutase;hydrogen peroxide;

Countries

China

Contacts

Public ContactZhu Yangzi

Xuzhou Central Hospital

zhuyz@188.com+86 181 6877 9150

Outcome results

None listed

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