Cancer
Conditions
Interventions
TEAS group 1:Continuous transcutaneous electrical acupoint stimulation 30 minutes before and during the operation
TEAS group 2:Giving transcutaneous electrical acupoint stimulation 3 to 5 days after the surgery
Control group:None
Sponsors
The First Affiliated Hospital of Wenzhou Medical University
Eligibility
Sex/Gender
All
Age
18 Years to 75 Years
Inclusion criteria
Inclusion criteria: (1)Laparoscopic radical resection of gastric, bowel, liver, lung, kidney, prostate cancer was performed under elective general anesthesia, and no metastatic lesions were found before operation; (2)ASA graded I-III grade, 18kg/m^2<BMI<= 31 kg/m^2, aged 18-75 years and no gender limitation; (3)No cognitive, communication disorders, mental disorders, able to communicate, understand and sign informed consent.
Exclusion criteria
Exclusion criteria: (1)There are surgical incisions or surgical scars, skin infections, nerve injuries in the local of the acupoint and the meridian, or a history of spinal surgery; (2)Participated in other clinical trials in the last four weeks; (3)Can't understand the NRS score, can't use the PCIA; (4)Having preoperative pain, central analgesics are being used or having opioid addiction, dependence; (5)Long-term use of hormone drugs and allergies; (6)People with liver and kidney problems(ALT, AST, BUN, Cr 1.5 above normal), K+>5.5mmol/L or K+<3.0mmol/L, preoperative Hb<7g/dl; (7)The researchers did not consider participants suitable for this trial.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The recurrence free survival ; | — |
Secondary
| Measure | Time frame |
|---|---|
| The CTC count;The Immune factor count;Complications 30 days after surgery;Overall survival time ;Postoperative NRS score; | — |
Countries
China
Contacts
Public ContactWang Junlu; Pan Yuanyuan
The First Affiliated Hospital of Wenzhou Medical University
Outcome results
None listed