Benign gallbladder disease
Conditions
Interventions
Intervention Group: Electroacupuncture intervention on meridian acupoints:The intervention involves providing Electroacupuncture intervention on meridian acupoints treatment on top of comprehensive in
Control group: Intervention with non-meridian and non-acupoint electric acupuncture.:The intervention involves providing electroacupuncture treatment on top of comprehensive intervention. The comprehe
Sponsors
Putuo Hospital, Shanghai University of Traditional Chinese Medicine
Eligibility
Sex/Gender
All
Age
18 Years to 70 Years
Inclusion criteria
Inclusion criteria: (1) Participants aged 18 to 70 years old, regardless of gender. (2) Diagnosed with benign gallbladder disease and meeting the indications for laparoscopic cholecystectomy outlined in the "Routine for Laparoscopic Cholecystectomy". (3) Signed informed consent form. (4) Having a physical status classified as Class III or better according to the criteria set by the American Society of Anesthesiologists, including the following three levels: Class I: Good physical health, normal development, and well-functioning organs; Class II: Mild coexisting illness excluding surgical diseases, with intact compensatory function; Class III: Severe coexisting illness, limited physical activity, but able to manage daily activities. (5) Undergoing abdominal surgery for the first time. Voluntarily participating in this clinical study. Only those who meet all the above criteria will be included.
Exclusion criteria
Exclusion criteria: (1) Patients requiring simultaneous combined surgeries. (2) Patients who convert to open surgery. (3) Patients who experience severe complications during or after surgery and require intensive care. (4) Patients who have used drugs affecting the intestines (such as herbal medicine) within one month. (5) Patients who have received acupuncture treatment within the past six months. (6) Patients with cardiac pacemakers. (7) Patients who are currently participating in other clinical studies within the past six months. (8) Patients with a history of syncope, epilepsy, or mental illness. (9) Patients undergoing epidural anesthesia. Exclusion will occur if any of the above criteria are met.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Postoperative abdominal distension grading;Postoperative abdominal distension VAS (Visual Analog Scale) scoring; | — |
Secondary
| Measure | Time frame |
|---|---|
| Time of resolution of postoperative abdominal distension;Postoperative pain, nausea, and vomiting;Time of first bowel gas passage after surgery;Time of first bowel movement after surgery;The length of stay in the hospital; | — |
Countries
China
Contacts
Public ContactWei Li
Putuo Hospital, Shanghai University of Traditional Chinese Medicine
Outcome results
None listed