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The association between dynamic cerebral autoregulation during abdominal major surgery in Trendelenburg position and postoperative delirium: a prospective cohort study

The association between dynamic cerebral autoregulation during abdominal major surgery in Trendelenburg position and postoperative delirium: a prospective cohort study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600122957
Enrollment
Unknown
Registered
2026-04-20
Start date
2026-05-01
Completion date
Unknown
Last updated
2026-04-27

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

Conditions

Postoperative delirium

Interventions

Postoperative delirium group and non-operative delirium group (Sample size per group depends on postoperative follow-up):None

Sponsors

The First Hospital of Lanzhou University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Aged >= 18 years; 2. American Society of Anesthesiologists Physical Status (ASA) I-III; 3. Scheduled to undergo major laparoscopic abdominal surgery under general anesthesia (including colorectal cancer resection, radical surgery, ovarian cancer staging, endometrial cancer radical surgery, cervical cancer radical surgery, myomectomy, etc.); 4. Voluntary participation in this study and provision of signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Pre-existing neuropsychiatric disorders such as schizophrenia, Parkinson's disease, epilepsy, or dementia, long-term use of psychiatric medications (e.g., antidepressants, antipsychotics), or a history of alcohol abuse within the recent past (1 month); 2. Preoperative cognitive impairment assessed by the Minimum Mental State Examination (MMSE) (score =30 kg/m^2; 4. Severe carotid artery stenosis (stenosis rate >=70%) or a history of carotid endarterectomy/stenting; 5. Acute cerebrovascular events (cerebral infarction, intracerebral hemorrhage, transient ischemic attack [TIA]) within the past 3 months; 6. Severe hepatic or renal insufficiency, severe cardiopulmonary dysfunction; 7. Inability to complete cognitive assessment due to severe visual or hearing impairment or language barriers.

Design outcomes

Primary

MeasureTime frame
Postoperative delirium (POD) defined by positive 3D-CAM assessment at any time point within 7 days postoperatively;

Secondary

MeasureTime frame
Time to extubation;Length of stay in PACU;Unplanned admission to ICU;Postoperative hospital length of stay;Postoperative complications (e.g., stroke, heart failure, pulmonary infection);Visual Analog Scale (VAS) pain score;Richmond Agitation-Sedation Scale (RASS) score;C-reactive protein (CRP);Albumin;Hemoglobin (Hb);Blood glucose;Electrolytes;Liver and renal function;

Countries

China

Contacts

Public ContactLiu Yatao

The First Hospital of Lanzhou University

liuyt@lzu.edu.cn+86 181 5210 7860

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 1, 2026