Visceral Pain
Conditions
Brief 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.
Detailed description
Patients aged 18-65 years old, BMI 18-30kg/m2, ASA grade I or II were selected for gynecologic laparoscopic surgery (laparoscopic ovarian tumor stripping, laparoscopic uterine fibroid stripping, laparoscopic total hysterectomy) under general anesthesia from May 2024 to July 2024. Exclusion criteria: Patients who were allergic to the drugs used in the study, had confusion or cognitive impairment, contraindicated 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. Exclusion criteria: patients dropped out of the experiment midway or the data was not completely collected, the surgical method changed midway, the operation duration was less than 30 minutes or more than 2 hours, and patients with opioid and addictive drug dependence
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
Sponsors
Yangzhou University
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
FEMALE
Age
18 Years to 65 Years
Healthy volunteers
Yes
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.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| the VAS score of postoperative visceral pain | 30 minutes after surgery、6 hours after surgery、24 hours after surgery、48 hours after surgery | 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. |
Countries
China
Contacts
Primary ContactMeiyu Liu
Outcome results
None listed