Effect of Electroacupuncture on Sepsis-induced Intestinal Dysfunction
Sepsis, Intestinal Dysfunction
About this trial
This is an interventional treatment trial for Sepsis focused on measuring sepsis, electroacupuncture, intestinal dysfunction
Eligibility Criteria
Inclusion Criteria:
- Meet the diagnostic criteria of sepsis 3.0
- AGI grade II or above,
- At least 18 years old
- Volunteer to participate in this study and sign the informed consent form
Exclusion Criteria:
- Patients with bowel dysfunction caused by other diseases or surgical operations
- Those who have chronic gastrointestinal diseases such as Crohn's disease and ulcerative colitis
- Those who have recently used gastrointestinal motility drugs and within 5 times the half-life
- Those who are participating in other drug clinical trials
- Refuse to participate in this study
Sites / Locations
- Electroacupuncture Apparatus
Arms of the Study
Arm 1
Arm 2
Experimental
Sham Comparator
electroacupuncture treatment
sham electroacupuncture treatment
Participants in the treatment group underwent 60 minutes acupuncture (0.30mm×70mm) at ST36 (Zusanli) and ST37 (Shangjuxu) twice a day for seven days. After"Deqi",electroacupuncture stimulation apparatus (HANS G6805-2, Huayi Co, Shanghai, China) isconnected and maintained the end of treatment
sham electroacupuncture treatment participants in the control group received shallow needling (0.30mm×25mm) at ST36 and ST37(nonacupoints located 1 inch beside acupoints, about 20mm). Specifically, the depth of needle insertion into nonacupoints is 3-5mm and avoided manual stimulation and no "Deqi" without actual current output.