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A time-effect study of transcutaneous electrical acupoint stimulation for the prevention of postoperative delirium

A time-effect study of transcutaneous electrical acupoint stimulation for the prevention of postoperative delirium

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600126495
Enrollment
Unknown
Registered
2026-06-10
Start date
2026-06-10
Completion date
Unknown
Last updated
2026-06-15

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

Conditions

Postoperative Delirium, POD

Interventions

TEAS group:In the experimental group, TEAS was applied to the Neiguan (PC6), Shenmen (HT7), Zusanli (ST36), and Taichong (LR3) acupoints starting 2 days before surgery, twice daily, with each session
Control group:In the control group, sham TEAS was applied, in which electrode pads were placed on the same acupoints and connected to the stimulator, but no electrical current was delivered.

Sponsors

The First Affiliated Hospital of Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

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

MeasureTime frame
POD incidence;

Secondary

MeasureTime 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

Public ContactLi Ping

The First Affiliated Hospital of Chongqing Medical University

202626@hospital.cqmu.edu.cn+86 130 6233 7738

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 21, 2026