Skip to content

The effect of transcutaneous auricular vagus nerve stimulation on postoperative delirium in elderly patients undergoing lower extremity orthopedic surgery

The effect of transcutaneous auricular vagus nerve stimulation on postoperative delirium in elderly patients undergoing lower extremity orthopedic surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600121372
Enrollment
Unknown
Registered
2026-03-30
Start date
2026-04-16
Completion date
Unknown
Last updated
2026-04-14

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

Conditions

Postoperative delirium

Interventions

The transcutaneous auricular vagus nerve stimulation group (taVNS) group:Place the stimulating electrode on the concha subvessel and another ear clip to the earlobe.
Control group:Two electrode clamps attached to the earlobe and the helix respectively

Sponsors

Hebei General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Patients aged >= 60; 2. ASA grade II or III; 3. Scheduled for elective lower extremity orthopedic surgery.

Exclusion criteria

Exclusion criteria: 1.Refuse to participate; 2.Preoperative cognitive impairment, defined as an MMSE score below education-adjustedcutoffs (<=17 for illiterate, <=20 for primary school, <=22 for middleschool, and<=23 for high school/college), based on previouslyvalidated normative and epidemiological evidence accountingfor the influence of education ; 3.Local auricular skin issues (rash, infection, lesions, ulcers, scars) 4.Patients with contraindications for taVNS, including implanted cardiac devices, a history of seizures, bleeding diathesis, or current anticoagulant use 5.Preoperative sinus bradycardia (HR < 60 bpm) and severe cardiovascular or cerebrovascular disease; 6.Airway hyperresponsiveness exists (e.g., asthma, chronic obstructive ventilatory dysfunction) 7.Pregnancy, or unable to cooperate with treatment; 8.Use of antibiotics, probiotics or prebiotics within 3 months before surgery; 9.History of gastrointestinal surgery, gastrointestinal disorders (e.g., peptic ulcer, diarrhea, or gastric bleeding).

Design outcomes

Primary

MeasureTime frame
The incidence of postoperative delirium;

Secondary

MeasureTime frame
Gut microbiota;Neutrophil extracellular trap biomarkers;Postoperative gastrointestinal function indicators;

Countries

China

Contacts

Public ContactZhang Meng

Hebei General Hospital

877109869@qq.com+86 311 8598 8127

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 17, 2026