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Clinical Study of Intestinal Barrier Dysfunction After Gastrointestinal Surgery

Clinical Study of Intestinal Barrier Dysfunction in Patients After Gastrointestinal Surgery

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06596070
Enrollment
180
Registered
2024-09-19
Start date
2024-10-31
Completion date
2025-04-30
Last updated
2024-09-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Intestinal Barrier Dysfunction

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?

Interventions

This study is an observational study and no intervention was performed on the patients.

Sponsors

The Second Affiliated Hospital of Kunming Medical University
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
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.

Design outcomes

Primary

MeasureTime frameDescription
operating timeDuring surgeryRecord the patient's surgical time

Secondary

MeasureTime frameDescription
bowel habitPreoperativeThe patient was asked whether there were increased frequency of stool, changes in stool characteristics, constipation and other conditions before surgery
Surgical ProceduresDuring surgeryRecord whether the patient underwent laparoscopic surgery or open surgery
hemorrhageDuring surgeryRecord the patient's intraoperative bleeding volume
AlbuminPreoperative and postoperative 24 hoursRecord the patient's albumin levels before and 24 hours after surgery
Infection indicatorsPreoperative and postoperative 24 hoursRecord the values of PCT, IL-6, and CRP of patients before and 24 hours after surgery
nutritional statusPreoperativePatients were assessed for risk of malnutrition by the Nutritional Risk Screening Scale (NRS-2002). A score of ≥3 indicated that the patient was at risk of malnutrition.
genderPreoperative
Body Mass IndexPreoperative
diabetesPreoperativeRecord whether the patient has diabetes
enteral nutritionThe average observation time is 2 weeks after surgery.Record the start time of enteral nutrition for patients after surgery.
Exhaust and defecation timeThe average observation time is one week after surgeryRecord the time of the patient's first exhaust and first bowel movement after surgery
agePreoperative

Contacts

Primary Contactweiming Li
liweiming49@163.com13114225597

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026