About this trial
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 criteria
This trial accepts healthy volunteersQualifiers
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.
Disqualifiers
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;
Trial design
Parallel
Treatments tested in this trial
TEAS
Other interventionBilateral 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
Oxycodone
DrugOxycodone 0.1mg/kg was injected intravenously 5 minutes before anesthesia induction
Treatment groups
Trial outcomes
Primary outcomes
the VAS score of postoperative visceral pain
the visual analogue scale of postoperative visceral pain,The basic method is to use a swimming scale about 10cm long, marked with 10 scales on one side, and "0" and "10" at each end, with 0 being painless and 10 being the most unbearable pain.
Sponsors and contacts
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