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The transcutaneous acupoint electrical stimulation performed at different perioperative timepoints for prevention of postoperative nausea and vomiting in high risk gynaecological patients undergoing laparoscopic surgery

The impact of Transcutaneous Acupoint Electrical Stimulation on high risk of Postoperative Nausea and Vomiting: Randomized, double-blind and controlled trial

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800018773
Enrollment
Unknown
Registered
2018-10-09
Start date
2018-10-15
Completion date
Unknown
Last updated
2020-03-02

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

Conditions

high risk of Postoperative Nausea and Vomiting in gynaecological patients undergoing laparoscopic surgery

Interventions

Group 1:preoperative TEAS
Group 2:preoperative TEAS combined with intraoperative TEAS
Group 3:postoperative TEAS
Group 4:sham TEAS

Sponsors

The First Affiliated Hospital of Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Patients with American Society of Anesthesiologists class I or III and scheduled for female Patients undergoing Gynaecological Laparoscopic Surgery

Exclusion criteria

Exclusion criteria: Contraindication of Transcutaneous Acupoint Electrical Stimulation, implantation of cardiac pacemaker, inability to understand the consent form, emergency, daily use of nsaids or hormones, pregnancy and Lactating woman; smoker.

Design outcomes

Primary

MeasureTime frame
incidence of nausea;incidence of vomiting;incidence of retching;need for rescue antiemetics;

Secondary

MeasureTime frame
operation and anaesthesia;time of the first postoperative flatus;pain intensity evaluated by VAS;10/5000 Postoperative complications;

Countries

China

Contacts

Public ContactMin Su

The First Affiliated Hospital of Chongqing Medical University

minsu89011068@163.com+86 13508302749

Outcome results

None listed

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