RecruitingNot Applicable

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

China120 participantsStarted 2024-05-01

Plain-language 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.

Who can participate

Age range18 Years – 65 Years

SexFEMALE

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * 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 Criteria: * 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.

What they're measuring

the VAS score of postoperative visceral pain

Timeframe: 30 minutes after surgery、6 hours after surgery、24 hours after surgery、48 hours after surgery

Trial details

NCT IDNCT06517069

SponsorYangzhou University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2025-06-01

Contact for this trial

Meiyu Liu

+86 177 6198 0727 myliu@yzu.edu

View on ClinicalTrials.gov More Visceral Pain trials