RecruitingNot ApplicableNCT06517069

Effect of TEAS Combined With Oxycodone on Postoperative Visceral Pain in Gynecologic Laparoscopic Patients

Effect of Transcutaneous Electrical Acupoint Stimulation Combined With Oxycodone on Postoperative Visceral Pain and Early Recovery Quality in Gynecologic Laparoscopic Patients

Sponsor

Yangzhou University

Enrollment

120 participants

Start Date

May 1, 2024

Study Type

INTERVENTIONAL

Conditions

Visceral Pain

Summary

To investigate the effect and feasibility of percutaneous acupoint stimulation combined with oxycodone on postoperative visceral pain in laparoscopic patients, and provided a clinical basis for optimizing perioperative pain management in laparoscopic patients.

Eligibility

Sex: FEMALEMin Age: 18 YearsMax Age: 65 Years

Inclusion Criteria4

Age 18-65 years
American Society of Anesthesiologists grade I-II
Body mass index (BMI) 18.5-30 kg/m2;
No ulceration or infection at the acupuncture stimulation site.

Exclusion Criteria6

Allergic to the drugs used in the study;
People with unclear consciousness or cognitive dysfunction;
There are contraindications of percutaneous acupoint electrical stimulation;
Abnormal cardiopulmonary and liver and kidney function;
History of analgesic drug use within one week;
History of diabetes, myocardial infarction or cerebrovascular accident.

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Interventions

OTHERTEAS

Bilateral Neiguan point (PC6), Zusanli point (ST36) and Sanyinjiao point (SP6) were selected. Use Huatuo electronic needle therapy device, Sulodine electric stimulation hand circle TEAS, Huatuo electronic needle therapy device parameter setting: Density wave, 2/10Hz, current intensity from weak to strong, until the patient can tolerate the maximum intensity (acid, numbness, distension, pain) is appropriate, after the Sulodine brand electrical stimulation bracelet is turned on, gradually increase the stimulation intensity, until the patient can tolerate the maximum intensity is appropriate, stimulation for 30min until anesthesia induction

DRUGOxycodone

Oxycodone 0.1mg/kg was injected intravenously 5 minutes before anesthesia induction