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Effects of percutaneous acupoint electrical stimulation on emergence agitation during recovery in patients undergoing kidney transplantation

Effects of percutaneous acupoint electrical stimulation on emergence agitation during recovery in patients undergoing kidney transplantation

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400081403
Enrollment
Unknown
Registered
2024-02-29
Start date
2023-04-11
Completion date
Unknown
Last updated
2024-03-04

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

Conditions

Emergence agitation

Interventions

Test group:Percutaneous acupoint electrical stimulation
control group:Non-percutaneous acupoint electrical stimulationon

Sponsors

Affiliated Hospital of Qingdao University
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.ASA ? ~III level; 2. Age =18 years old; 3. Volunteer to join the study.

Exclusion criteria

Exclusion criteria: 1. Cognitive dysfunction was identified by using the simple mental State scale before surgery; 2. The fuzzy consciousness assessment suggests delirium; 3. Local skin infection, chronic inflammation or inability to apply electrodes on the surface of acupuncture point stimulation site; 4. Difficult airway, severe pulmonary complications and airway hyperreactivity are expected to have a greater impact on postoperative tracheal extubation.

Design outcomes

Secondary

MeasureTime frame
VAS pain score;—

Primary

MeasureTime frame
Ramsay sedation score during recovery;RSS agitation score;—

Countries

China

Contacts

Public ContactChai Dongyue

Department of Anesthesiology, Affiliated Hospital of Qingdao University

chaidongyue@qdu.edu.cn+86 186 6180 3006

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026