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

ConditionVisceral Pain
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-65
SponsorYangzhou University

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 volunteers

Qualifiers

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

Design model

Parallel

Treatments tested in this trial

  • TEAS

    Other intervention

    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

  • Oxycodone

    Drug

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

Treatment groups

120 Participants
are divided into 4 treatment groups
Group A: TEAS combined with OxycodoneExperimental treatment 2 interventions
Group B: TEASExperimental treatment 1 intervention
Group C: OxycodoneExperimental treatment 1 intervention
Group D: ComparatorNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

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.

Time frame
30 minutes after surgery、6 hours after surgery、24 hours after surgery、48 hours after surgery

Secondary outcomes

Other outcomes

Sponsors and contacts

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