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The effect of desflurane or propofol used for general anesthesia maintenance on postoperative delirium in elderly patients with cognition frailty

The effect of desflurane or propofol used for general anesthesia maintenance on postoperative delirium in elderly patients with cognition frailty

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400082942
Enrollment
Unknown
Registered
2024-04-11
Start date
2023-12-01
Completion date
Unknown
Last updated
2024-04-15

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

Conditions

Postoperative Delirium

Interventions

group D:After using the same induction anesthesia regimen, both groups were anesthetized with inhalation of desflurane, and the concentration of desflurane was adjusted to maintain a BIS value between
group P:After using the same induction anesthesia regimen, both groups were infused with propofol to maintain anesthesia and maintain BIS values between 40 and 60

Sponsors

The First Affiliated Hospital of Chongqing Medical University,Chongqing ,China
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 120 Years

Inclusion criteria

Inclusion criteria: (1) Age = 65 years old, planning to undergo elective tracheal intubation for general anesthesia surgery; (2) Accepting hip or knee replacement surgery; (3) American Society of Anesthesiologists Classification (ASA Classification): II-III; (4) Sign a written informed consent form; (5) FFP = 3; (6) MMSE 17 points, primary school > 20 points, high school and above > 22 points, university and above > 23 points).

Exclusion criteria

Exclusion criteria: (1) Having a family history of malignant high fever or having experienced malignant high fever; (2) A history of allergies to propofol or desflurane; (3) Plan to postpone tracheal extubation; (4) Those with severe visual and auditory impairments who cannot cooperate; (5) Having a definite diagnosis of neurological diseases or mental disorders (such as Parkinson's disease, dementia, schizophrenia, or depression); (6) Delirium has already existed before surgery (evaluated using the 3D-CAM scale on the day before surgery, see Appendix 3 for details); (7) Long term use of anticholinergic drugs or other drugs that affect the central nervous system before surgery; (8) Participate in other clinical studies within 3 months.

Design outcomes

Primary

MeasureTime frame
Postoperative Delirium;

Secondary

MeasureTime frame
Postoperative recovery time;Tracheal tube extraction time;Time to reach PACU exit standard;The incidence of hypoxemia after extubation;The incidence of nausea and vomiting within 5 days after surgery;Pain level within 24 hours after surgery;Total hospitalization time;Readmission rate within 30 days;Postoperative complications rate;

Countries

China

Contacts

Public ContactJuYing Jin

Departmentof Anesthesiology,The First Affiliated Hospital of Chongqing Medical University,Chongqing ,China

juyingjin@hotmail.com+86 135 2748 6171

Outcome results

None listed

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