Uterine fibroids, adenomyosis, endometriosis
Conditions
Interventions
Group A: control group (Sham TEAS + saline) :30 minutes before induction of anesthesia, 1 day and 2 days after operation, the dominant side of Neiguan and He were selected.
Sham TEAS ( target acupoin
Group B: drug group (Sham TEAS + metoclopramide):30 minutes before induction of anesthesia, 1 day and 2 days after operation, the dominant side of Neiguan and He were selected.
Sham TEAS ( target acu
Group C: combination group (TEAS + metoclopramide):30 minutes before induction of anesthesia, 1 day and 2 days after operation, the dominant side of Neiguan and He were selected.
TEAS was performed a
Sponsors
The First Affiliated Hospital of Gannan Medical University
Eligibility
Sex/Gender
Female
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: 1: Patients undergoing elective gynecological laparoscopic surgery 2: Age : 18-65 years 3: BMI:18 .5-28Kg / m^2 4: ASA grade I-II 5: Signing informed consent
Exclusion criteria
Exclusion criteria: 1: Pregnancy or Lactation 2: For those who are allergic or intolerant to the study drugs 3: There are ulcers or infections around the target acupoints 4: Nausea, vomiting or both within 24 hours before operation 5: Patients who used opioids, glucocorticoids, emetics or antiemetic drugs within 24 hours before surgery 6: People with vestibular disorders, neurological or psychiatric disorders, severe liver or kidney dysfunction 7: There is extravertebral motor disease 8: Participate in other researchers within 3 months
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The incidence of postoperative nausea and vomiting within 24 hours after operation;Adverse events (treatment related/unrelated); | — |
Secondary
| Measure | Time frame |
|---|---|
| The incidence of PON, POV, PONV and severity of nausea and the number of vomiting/dry heaves were recorded for 0-2h, 2-6h, 6-24h, and 24-48h postoperatively.;Postoperative pain VAS scores, use of remedial antiemetic (ondansetron) versus opioids during the 48h postoperative period were recorded, and patient satisfaction was assessed after 48h postoperatively.;The operation time, anesthesia time, extubation time, recovery time, total hospital stay, intraoperative propofol dosage, remifentanil dosage, intraoperative bleeding, and fluid infusion were recorded.;Basic patient information was recorded: age, height, weight, BMI, smoking history, history of motion sickness/PONV, and type of surgery.; | — |
Countries
China
Contacts
Public ContactLifeng Wang
The First Affiliated Hospital of Gannan Medical University
Outcome results
None listed