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

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

Treatments tested in this trial

  • TEAS
  • Oxycodone

Treatment groups

120 Participants
are divided into 4 treatment groups

Sponsors and collaborators