Effect of Electroacupuncture on SAP With MODS
Severe Acute Pancreatitis
About this trial
This is an interventional treatment trial for Severe Acute Pancreatitis focused on measuring Severe Acute Pancreatitis, Multiple Organ Disfunction Syndrome
Eligibility Criteria
Inclusion Criteria:
- Meet the diagnosis of severe acute pancreatitis (Atlanta diagnostic criteria), within 1 week of onset
- Combine 2 or more organ failures at the same time, and the duration is greater than 48h
- Age ≥18 years old;
- Obtain informed consent.
Exclusion Criteria:
- Pregnancy pancreatitis;
- Patients who have undergone percutaneous puncture or surgical drainage before admission, and have undergone surgical decompression due to early abdominal hypertension;
- Patients with a history of chronic organ dysfunction (such as uremia, COPD, liver cirrhosis, heart failure, etc.).
- Those who have a medical history of acupuncture and moxibustion or are not sensitive to acupuncture and moxibustion.
- Those who refuse to participate in the research
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Experimental
Sham Comparator
electroacupuncture treatment
sham electroacupuncture treatment
Participants in the treatment group underwent 30 minutes acupuncture (0.30mm×70mm) at Zusanli(ST36), Xiajuxu(ST39), Hegu(LI4), Neiguan(PC6) once a day for seven days. After"Deqi",electroacupuncture stimulation apparatus (HANS G6805-2, Huayi Co, Shanghai, China) isconnected and maintained the end of treatment.
Participants in the control group received shallow needling (0.30mm×25mm) at nonacupoints (located 1 inch beside acupoints). Specifically, the depth of needle insertion into nonacupoints is 3-5mm and avoided manual stimulation and no "Deqi" without actual current output.