Correlation Study Between SMA Blood Flow Reactivity and Acute Gastrointestinal Injury in Critically Ill Patients
NCT ID: NCT07001943
Last Updated: 2025-09-05
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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RECRUITING
80 participants
OBSERVATIONAL
2025-06-01
2026-07-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Interventions
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enteral nutrition
We'll use an enteral nutrition intervention with intact protein formulations. Initiate nasogastric tube feeding at 20ml/h and continue for 24 hours. Adjust feeding strategies based on patients' SMA blood flow reactivity.
Eligibility Criteria
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Inclusion Criteria
* Admitted to the study with a expected stay of more than 72 hours.
* Require initiation of enteral nutrition support.
Exclusion Criteria
* Patients with gastrointestinal bleeding.
* Patients with bowel obstruction.
* Pregnant or lactating women.
* Patients with contraindications to bedside Doppler ultrasound.
18 Years
80 Years
ALL
No
Sponsors
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Peking Union Medical College Hospital
OTHER
Responsible Party
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Locations
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Peking union medical college hospital
Beijing, Beijing Municipality, China
Countries
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Facility Contacts
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Other Identifiers
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SMART(SMA Reactivity Trial)
Identifier Type: -
Identifier Source: org_study_id
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