Clinical Study of Intestinal Barrier Dysfunction After Gastrointestinal Surgery
NCT ID: NCT06596070
Last Updated: 2024-09-19
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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NOT_YET_RECRUITING
180 participants
OBSERVATIONAL
2024-10-31
2025-04-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_CONTROL
PROSPECTIVE
Study Groups
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Intestinal barrier dysfunction group
No intervention was carried out
This study is an observational study and no intervention was performed on the patients.
Non-intestinal barrier dysfunction group
No intervention was carried out
This study is an observational study and no intervention was performed on the patients.
Interventions
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No intervention was carried out
This study is an observational study and no intervention was performed on the patients.
Eligibility Criteria
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Inclusion Criteria
* 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
* 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.
18 Years
80 Years
ALL
No
Sponsors
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The Second Affiliated Hospital of Kunming Medical University
OTHER
Responsible Party
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Weiming Li
Investigator
Central Contacts
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Other Identifiers
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PJ-2024-124
Identifier Type: -
Identifier Source: org_study_id
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