Uterine fibroids
Conditions
Interventions
Control group:no
Experimental group:Transcutaneous electrical acupoint stimulation
Sponsors
Department of Anesthesiology, the First Affiliated Hospital of Wenzhou Medical University
Eligibility
Sex/Gender
Female
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: 1. Female patients aged 18-60 years; 2. ASA graded I-II grade, 18kg/m^2<=BMI<=30 kg/m^2; 3. The preoperative diagnosis was clearly uterine leiomyoma; 4. Elective laparoscopic myomectomy; 5. Volunteer to participate in this research and signed an informed consent form; 6. The ability to understand and communicate is normal.
Exclusion criteria
Exclusion criteria: 1. Patients with any surgical incisions, surgical scars, wounds, ulcers in the meridians in Hegu/ Neiguan/ Sanyinjiao/ Zusanli, or patients with skin infections in the meridian points; 2. Have a history of upper or lower limb nerve injury or previous spinal surgery; 3. In the menstrual period or breast-feeding period; 4. History of Meniere's disease; 5. Complicated with pain before the operation, analgesic drugs are being used; 6. Patients who are addicted or dependent on opioids; 7. Patients with severe heart, brain, lung, liver, and kidney diseases; 8. People with mental illness or language communication and understanding barriers.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The rate of cough response during anesthesia induction;The rate of propofol injection pain during anesthesia induction;Hemodynamics in surgery;40-item recovery quality rating scale; | — |
Countries
China
Contacts
Public ContactWang Junlu
Department of Anesthesiology, the First Affiliated Hospital of Wenzhou Medical University
Outcome results
None listed