Postoperative Delirium, POD
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Patients scheduled to undergo elective hip or knee arthroplasty under general anesthesia; 2) Age >=65 years; 3)Voluntary informed consent signed
Exclusion criteria
Exclusion criteria: 1) Contraindications to transcutaneous electrical stimulation, including local skin damage, infection, or presence of an implanted electrophysiological device; 2) Communication disorders or inability to cooperate with the investigator (e.g., due to psychiatric illness); 3) Life-threatening conditions or unstable vital signs; 4) Preexisting dementia, delirium symptoms, or cognitive impairment before intervention; 5) Substance abuse or dependence; 6) Participation in another clinical trial within 3 months prior to enrollment in this study; 7) Other conditions deemed unsuitable for inclusion by the investigator.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| POD incidence; | — |
Secondary
| Measure | Time frame |
|---|---|
| Daily pain score;Postoperative sedative and analgesic consumption;Sleep quality score;Time to first oral water intake;Time to first oral food intake;Time to first ambulation;Postoperative complications;Inflammatory markers; | — |
Countries
China
Contacts
The First Affiliated Hospital of Chongqing Medical University