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Effects of Transcutaneous Electrical Acupoint Stimulation on Perioperative Sleep Quality in Patients Undergoing Gynecological Surgery

Effects of Transcutaneous Electrical Acupoint Stimulation on Perioperative Sleep Quality in Patients Undergoing Gynecological Surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026000797
Enrollment
Unknown
Registered
2026-03-27
Start date
2026-04-01
Completion date
Unknown
Last updated
2026-04-28

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

Conditions

Sleep Disorders After Gynecological General Anesthesia Surgery

Interventions

experimental group:Transcutaneous Electrical Acupoint Stimulation (TEAS)
matched group: fake acuouncture

Sponsors

Qilu Hospital of Shandong University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria: 1.Female patients aged 18–65 years. 2.Scheduled to undergo elective gynecological surgery under general anesthesia.

Exclusion criteria

Exclusion criteria: Exclusion criteria: 1. ASA classification > III 2. BMI > 30 kg/m² or 2 times the upper limit of normal; or creatinine clearance < 30 ml/min) 6. Pregnant or breastfeeding women 7. Participation in other clinical trials within the past month that may interfere with the interpretation of results 8. Received acupuncture treatment within the past two months

Design outcomes

Primary

MeasureTime frame
Total Sleep Time (TST) recorded by a sleep monitoring;—

Secondary

MeasureTime frame
pittsburgh sleep quality index,PSQI;VAS;AIS;—

Countries

China

Contacts

Public Contactwangchunling

Qilu Hospital of Shandong University

wchl2000@163.com+86 185 6008 3819

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: May 1, 2026