Clinical Study of Intestinal Barrier Dysfunction After Gastrointestinal Surgery

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-80
SponsorThe Second Affiliated Hospital of Kunming Medical University

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

Treatment groups

180 Participants
are divided into 2 treatment groups

Locations

This trial has no locations