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acupoint stimulation of ST36 and PC6 on postoperative and vomiting in patients undergoing gynecological laparoscopic surgery: a randomized,double-blind,controlled,prospective study

acupoint stimulation of ST36 and PC6 on postoperative and vomiting in patients undergoing gynecological laparoscopic surgery: a randomized,double-blind,controlled,prospective study

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2200006787
Enrollment
Unknown
Registered
2022-11-16
Start date
2022-12-01
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 nausea and vomiting

Interventions

T3:TEAS 30mins before induction of anesthesia + continuous TEAS from intraoperative CO2 pneumoperitoneum intake to the end of surgery + TEAS 30 mins 1 day after surgery
T1:TEAS 30mins before induction of anesthesia
C:Before induction of anesthesia, electrodes were applied in ST36 and P6 to give 1mA electrical stimulation for 30mins. After induction of anesthesia, no electrical stimulation was performed until the
T2:TEAS 30mins before induction of anesthesia + TEAS 30mins 1 day after surgery

Sponsors

Zhongnan Hospital of Wuhan University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria :(1) 18 years old-70 years old (2) BMI: 18-31 kg/m2 (3) Elective surgery of uterus or appendages was performed under laparoscopy under general anesthesia, 0= operation time =3 hours (4) American Society of Anesthesiologists ASA Class ?-? (5) Volunteer to sign the clinical trial consent form

Exclusion criteria

Exclusion criteria: Exclusion criteria :(1) patients with severe diseases of circulatory system, urinary system, blood system or central nervous system (2) Preoperatively diagnosed digestive diseases affecting gastrointestinal motility, such as gastroduodenal ulcer, chronic constipation, irritable bowel syndrome, ulcerative colitis, etc(3) Use antiemetic or gastrointestinal motility drugs 1 day before surgery (4) Skin infection and damage at acupoints and intolerance to acupoint stimulation treatment, poor compliance (5) Patients with motion sickness and smoking history (6) Conversion to open surgery

Design outcomes

Primary

MeasureTime frame
Incidence of postoperative nausea and vomiting;

Secondary

MeasureTime frame
Abdominal bloating scores;

Countries

china

Contacts

Public ContactWU Yun
2233051659@qq.com18071121132

Outcome results

None listed

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