postoperative ileus after Radical Gastrectomy
Conditions
Interventions
Transcutaneous auricular vagus nerve stimulation group:Accept bilateral TEAS auricular internal organ area/auricle area, with normal instrumentation for stimulation. Interventions are carried out at 2
Sham Transcutaneous Vagus Nerve Stimulation Group:Subjects assigned to the ShamTEAS auricular acupoint group will receive sham stimulation, with the stimulation device being a placebo stimulator. The
Sponsors
Qilu Hospital of Shandong University(Qingdao)
Eligibility
Sex/Gender
All
Age
18 Years to 75 Years
Inclusion criteria
Inclusion criteria: (1) Pathologically diagnosed gastric cancer (stage I-III), American Society of Anesthesiologists (ASA) grade I-III, and planned to undergo elective laparoscopic gastrectomy; (2) Age: 18-75 years old, gender is not limited; (3) Patients who voluntarily or their families agree to participate in the trial and sign the informed consent form for the trial.
Exclusion criteria
Exclusion criteria: 1. History of previous abdominal surgery; 2. Plan for palliative resection, emergency surgery, or combined resection of other organs (such as liver, pancreas); 3. Discovery of serious complications intraoperatively necessitating conversion to open surgery (such as massive bleeding, anastomotic leak); 4. Presence of non-cancerous gastric lesions (confirmed by postoperative pathology); 5. Serious postoperative complications occurring during the study requiring a second surgery; 6. Comorbidities of severe cardiac, hepatic, renal diseases, or mental illness; 7. Local skin infections preventing the placement of electrodes; 8. Patients with permanent cardiac pacemakers installed; 9. Pregnant or breastfeeding women; 10. Individuals unable to maintain a resting state (such as those with epilepsy, Parkinson's disease, etc.); 11. Patients or their family members unwilling to sign the informed consent form for the trial.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| First exhaust time; | — |
Secondary
| Measure | Time frame |
|---|---|
| First bowel movement time;The incidence of POI extension;Timing of water intake ;Liquid diet tolerance time;Solid food tolerance time;Number of episodes of nausea, vomiting, and bloating;Severity of postoperative pain;First out-of-bed time;First independent walking time;Length of postoperative hospital stay;Nutritional Risk Screening (NRS-2002);Quality of Life Questionnaire;Adverse events (AEs);Severe complications; | — |
Countries
China
Contacts
Public ContactFeng Li
Qilu Hospital of Shandong University(Qingdao)
Outcome results
None listed