About this trial
The goal of this observational study is to explore the clinical influences associated with the development of intestinal barrier dysfunction in patients undergoing gastrointestinal surgery. The main question it aims to answer is:What clinical factors increase the probability of developing intestinal barrier dysfunction in patients after gastrointestinal surgery?
Eligibility criteria
Qualifiers
men or women aged 18-80 years
expected feasible abdominal surgical treatment (partial gastrectomy, colorectal resection)
no preoperative intestinal barrier dysfunction
patients voluntarily participated in this study and signed an informed consent form.
Disqualifiers
Patients or their families refused to participate in this study
chronic inflammatory diseases (e.g. inflammatory bowel disease, chronic hepatitis, chronic pancreatitis, chronic peptic ulcer, etc.)
history of antibiotic administration in the last 2 weeks
severe cognitive impairment and other inability to cooperate preoperative neoadjuvant radiotherapy
Trial design
Treatments tested in this trial
- No intervention was carried out