Acute gastrointestinal disorder with sepsis
Conditions
Interventions
Experimental group :Liangge Powder Decoction
Control group:Blank control
Sponsors
Shuguang Hospital affiliated to Shanghai University of TCM
Eligibility
Sex/Gender
All
Age
18 Years to 85 Years
Inclusion criteria
Inclusion criteria: 1) Patients who meet the diagnostic criteria of Western medicine for acute gastrointestinal disorders of sepsis; 2) AGI level I-III; 3) People between the ages of 18 and 85, regardless of gender; 4) Gastrointestinal safety, no enteral nutrition (EN) contraindications; 5) Patients and/or immediate family members understand and agree to this study and sign informed consent.
Exclusion criteria
Exclusion criteria: 1) in the terminal stage of various diseases; 2) The primary disease is gastrointestinal disease, such as peptic ulcer, atrophic gastritis, and gastrointestinal resection, gastrointestinal or abdominal surgery recovery; 3) patients with malignant tumors; 4) Mental illness; 5) Pregnant and lactating women; 6) Patients with severe allergy to Chinese medicine; 7) Patients with antibiotic application that has a greater impact on gastrointestinal tract were excluded.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Acute gastrointestinal injury grading; | — |
Secondary
| Measure | Time frame |
|---|---|
| 28-day survival rate;Acute Physiology and Chronic Health Evaluation;Classification of bowel sounds;Gastric residual volume;Sequential organ failure score;D-lactic acid;Diamine oxidase;Endotoxin; | — |
Countries
China
Contacts
Public ContactYue Jin
Shuguang Hospital affiliated to Shanghai University of TCM
Outcome results
None listed