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Clinical Trials/NCT06596070
NCT06596070Not yet recruitingNot Applicable

Clinical Study of Intestinal Barrier Dysfunction in Patients After Gastrointestinal Surgery

The Second Affiliated Hospital of Kunming Medical University0 sites180 target enrollmentStarted: October 2024Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Enrollment
180
Primary Endpoint
operating time

Study Overview

Brief Summary

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?

Study Design

Study Type
Observational
Observational Model
Case Control
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to 80 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • 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.

Exclusion Criteria

  • 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
  • combined with severe hepatic, renal, and cardiac insufficiency patients.

Outcomes

Primary Outcomes

operating time

Time Frame: During surgery

Record the patient\'s surgical time

Secondary Outcomes

  • nutritional status(Preoperative)
  • bowel habit(Preoperative)
  • Surgical Procedures(During surgery)
  • hemorrhage(During surgery)
  • Albumin(Preoperative and postoperative 24 hours)
  • Infection indicators(Preoperative and postoperative 24 hours)
  • age(Preoperative)
  • gender(Preoperative)
  • Body Mass Index(Preoperative)
  • diabetes(Preoperative)
  • enteral nutrition(The average observation time is 2 weeks after surgery.)
  • Exhaust and defecation time(The average observation time is one week after surgery)

Investigators

Sponsor
The Second Affiliated Hospital of Kunming Medical University
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Weiming Li

Investigator

The Second Affiliated Hospital of Kunming Medical University

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