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Acupoint stimulation for relieving postoperative agitation in children-a randomized controlled clinical trial

Clinical study on acupoint stimulation to relieve postoperative agitation in children

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2200006695
Enrollment
Unknown
Registered
2022-10-10
Start date
2022-10-10
Completion date
Unknown
Last updated
2023-02-20

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

Conditions

postoperative agitation

Interventions

LI11+ST36:Transcutaneous electrical stimulation on acupoints
HT7+LR3:Transcutaneous electrical stimulation on acupoints
Sham:Apply the electrode on the acupoint without stimulation

Sponsors

Shenzhen Traditional Chinese Medicine Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: ? Children aged 1-7 who are hospitalized in Shenzhen Traditional Chinese Medicine Hospital and plan to undergo short surgery (operation time < 2h) with sevoflurane anesthesia ? Apgar score = 8 ? ASA is classified as Grade I-II ? Informed consent has been signed

Exclusion criteria

Exclusion criteria: ? Cardio, pulmonary and brain surgery or severe cardio, pulmonary and brain disease ? History of dystocia or perinatal cerebral ischemia and hypoxia ? Gestational age = 30 weeks ? Diagnosed neurodevelopmental retardation ? Participated in or is participating in other clinical studies 3 months before enrollment

Design outcomes

Primary

MeasureTime frame
Incidence rate and score of postoperative agitation;—

Countries

China

Contacts

Public ContactFengyan Shen
sfy3200@gzucm.edu.cn0755-88359666 -2505

Outcome results

None listed

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