Status:
NOT_YET_RECRUITING
Effect of Acupoint Stimulation on Postoperative Delirium and Electroencephalogram
Lead Sponsor:
Zhihong LU
Conditions:
Anesthesia
Postoperative Delirium
Eligibility:
All Genders
65+ years
Phase:
NA
Brief Summary
Transcutaneous electrical acupoint stimulation (TEAS) was reported to benefit the patients undergoing surgeries by reducing anesthetics consumption and decreasing anesthesia related adverse effects. E...
Eligibility Criteria
Inclusion
- aged 65 years or older
- American Society of Anesthesiologists (ASA) classification≤ Grade III
- Patients scheduled for elective abdominal surgery under general anesthesia
- Informed consent
Exclusion
- Patients with severe central nervous system injury or severe cerebrovascular disease
- Patients with cognitive dysfunction assessed by Confusion Assessment Method before surgery
- Patients unable to cooperate with studies, such as psychiatric disorders or difficulty in communication
- Patients with severe hepatic and renal insufficiency
- Patients with severe respiratory diseases
- Patients with contraindication for transcutaneous electrical stimulation, such as implanted electrophysiological devices, skin infection and damage at acupuncture points
- Anticipated duration of anesthesia shorter than 2 hours or postoperative hospital stay shorter than 3 days
Key Trial Info
Start Date :
December 10 2023
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
June 1 2026
Estimated Enrollment :
226 Patients enrolled
Trial Details
Trial ID
NCT06161662
Start Date
December 10 2023
End Date
June 1 2026
Last Update
December 8 2023
Active Locations (1)
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1
the First Affiliated Hospital of the Air Force Military Medical University
Xi'an, Shaanxi, China, 710032