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the influence of different anesthesia maintenance methods on postoperative delirium in elderly patients undergoing non-cardiac surgery

the influence of different anesthesia maintenance methods on postoperative delirium in elderly patients undergoing non-cardiac surgery:a prospective, randomized, placebo, three-arm clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600119936
Enrollment
Unknown
Registered
2026-03-05
Start date
2026-06-01
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Postoperative delirium

Interventions

TIVA group(total-intravenous anesthesia group):intravenous administrations of propofol (4 - 12mg/kg/h) or ciprofol (0.8 - 2.4 mg/kg/h)
IHA group(inhalational anesthesia group):inhalation anesthesia of desflurane of sevoflurane
CIVIA group(combination of intravenous anesthesia and inhalation anesthesia ):combination anesthesia of inhalation and intravenous administration

Sponsors

Ruijin Hospital, Shanghai Jiao Tong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
80 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Provision of written informed consent; 2.Planned for elective non-cardiac surgery; 3.Patients of American Society of Anesthesiologists physical status I-IV (ASA I-IV). 4.Duration of surgery lasting over 1hour; 5.Aged over 80;

Exclusion criteria

Exclusion criteria: 1.Patients undergoing emergency, ambulatory, cardiac, or neurosurgical procedures. 2.Body mass index (BMI) = 45kg/m2; 3.Chronic use of sedatives, antidepressants, or hypnotics; 4.Inability to complete cognitive assessments due to hearing impairment, language barriers, or other communication limitations; 5.History of malignant hyperthermia; 6.Neuromuscular disease; 7.Alcohol or substance abuse; 8.Any condition that the investigator considers incompatible with safe participation or reliable follow-up;

Design outcomes

Primary

MeasureTime frame
the incidence of postoperative delirium;

Secondary

MeasureTime frame
severity of postoperative delirium;Sleep quality;Length of stay in the ICU;Long-term postoperative changes in cognitive function;Pain scores;PONV;Intraoperation hypotension;Requirement for supplemental oxygen;All-cause mortality;Recovery quality;Length of stay in hospital;

Countries

China

Contacts

Public ContactQianzi Yang

Ruijin Hospital, Shanghai Jiao Tong University School of Medicine

qianziyang@hotmail.com+86 191 0212 3726

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 11, 2026