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Study on Prevention and Treatment of Postoperative Nausea and Vomiting with Transcutaneous Electrical Acupoint Stimulation in High-Risk Patients Undergoing Gynecological Laparoscopic Surgery

Study on Prevention and Treatment of Postoperative Nausea and Vomiting with Transcutaneous Electrical Acupoint Stimulation in High-Risk Patients Undergoing Gynecological Laparoscopic Surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026000460
Enrollment
Unknown
Registered
2026-03-05
Start date
2023-12-01
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

Postoperative nausea and vomiting

Interventions

Group S1 (Transcutaneous Acupuncture Point Electrostimulation Group):Thirty minutes before anesthesia induction, thirty minutes before the end of surgery, and after removal of the laryngeal mask, bila
Group S0 (Sham electrostimulation group):Group S0 had adhesive electrode patches applied at the same time points and acupuncture points, connected to an electrical stimulator, but without activating t

Sponsors

Guizhou University of Traditional Chinese Medicine Second Affiliated Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) Patients scheduled for gynecological laparoscopic surgery under general anesthesia; (2) Patients identified as having the qi deficiency, yang deficiency, or blood stasis constitutions based on the Chinese medicine constitution questionnaire; (3) Patients aged 18 to 65 years; (4) Patients classified as ASA I or II.

Exclusion criteria

Exclusion criteria: (1) Patients refuse; (2) Patients who cannot cooperate to complete the constitution survey questionnaire; (3) Patients with recent central nervous system diseases, gastrointestinal diseases, or vestibular system diseases that can cause nausea and vomiting; (4) Patients who received antiemetic treatment or had a gastric tube placed within 1 week before surgery; (5) Patients with skin lesions or infections near the selected acupoints; (6) Surgical duration exceeding 3 hours.

Design outcomes

Primary

MeasureTime frame
The incidence of nausea and vomiting, and the severity of PONV in two groups of patients during the postoperative periods of 0-6 hours, 6-12 hours, 12-18 hours, and 18-24 hours.;

Secondary

MeasureTime frame
Serum 5-HT levels in both groups of patients upon entering the operating room and 12 hours postoperatively, postoperative use of rescue antiemetic drugs, and time to first flatus.;Record patient demographics, Apfel score, duration of surgery and anesthesia, intraoperative fluid administration, anesthesia drug usage, total time in PACU, and total hospital stay duration. D records mean arterial pressure (MAP), heart rate (HR), oxygen saturation (SpO2), and Bispectral Index (BIS) at three time points: upon entering the operating room (T1), at skin incision (T2), and at the end of surgery (T3).;

Countries

China

Contacts

Public ContactSong Jing

Guizhou University of Traditional Chinese Medicine Second Affiliated Hospital

351070441@qq.com18885072254

Outcome results

None listed

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