Effect of percutaneous acupoint electrical stimulation combined with opioid-free anesthesia on gastrointestinal function after laparoscopic gynecological surgery

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2400080539

Enrollment

Unknown

Registered

2024-01-31

Start date

2024-02-01

Completion date

Unknown

Last updated

2024-02-05

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

Conditions

opioid-free anesthesia

Interventions

Tgroup:TEAS combined with opiate-free anesthesia

Contral group:sham TEAS combined with opiate-based anesthesia

Eligibility

Sex/Gender

Female

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Gynecological patients undergoing elective laparoscopic surgery (ASA Grade I-III)

Exclusion criteria

Exclusion criteria: Refusal to participate, cotting disorders, local infections, allergies, pacemaker implants

Design outcomes

Primary

Measure	Time frame
Postoperative nausea and vomiting;	—

Secondary

Measure	Time frame
Postoperative pain;Analgesic remedy;Side events;	—

Countries

China

Contacts

Public ContactQihong Shen

Affiliated Hospital of Jiaxing University

shenqihong1989@163.com+86 150 8855 4023

Outcome results

None listed

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