Clinical trial Recruiting at 1 site Observational Ages 18 to 80

Monitoring intestinal blood flow after feeding to predict gut injury in critically ill patients

Official title: Correlation Study Between SMA Blood Flow Reactivity and Acute Gastrointestinal Functional Injury in Critically Ill Patients

Run by Peking Union Medical College Hospital · NCT07001943 · Data updated 2026-11-12

We will test whether bedside Doppler measurements of superior mesenteric artery blood flow after enteral feeding can predict acute gastrointestinal injury in adult ICU patients.

More Critical Illness trials

Quick facts

Study typeObservational
Ages18 Years to 80 Years
SexAll
Enrollment80 (estimated)
SponsorPeking Union Medical College Hospital
Academic / other
Locations1 site (Beijing, Beijing Municipality)
StatusRecruiting
StartedJune 1, 2025
Main results expectedJune 1, 2026
Study endsJuly 1, 2026
Registry record updatedSeptember 5, 2025
Trial IDNCT07001943 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults 18–80 years old admitted to the ICU at Peking Union Medical College Hospital with an expected stay >72 hours who require initiation of enteral nutrition and have no contraindications to bedside Doppler.

Probably not a fit

Patients with pre-existing severe gastrointestinal disease, active gastrointestinal bleeding, bowel obstruction, pregnancy or lactation, or contraindications to Doppler ultrasound may not receive benefit from this approach.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study will use bedside Doppler ultrasound to measure superior mesenteric artery (SMA) blood flow before and after enteral feeding in adult ICU patients. Investigators will record SMA flow changes alongside standard hemodynamic measurements and clinical markers of acute gastrointestinal injury (AGI). They will analyze patterns of SMA reactivity, develop a predictive model linking SMA changes to AGI risk, and explore how those findings could inform individualized enteral nutrition strategies. All data collection will occur in the ICU at Peking Union Medical College Hospital for patients who meet eligibility criteria.

Why it matters

Potential benefit: If successful, this approach could enable personalized enteral feeding that reduces AGI incidence and improves ICU outcomes.

How similar studies have gone: Prior research shows SMA blood flow changes with feeding and relates to intestinal perfusion, but using bedside SMA reactivity specifically to predict AGI and guide individualized enteral nutrition is relatively novel and not yet widely validated.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Adults aged ≥18 years and ≤80 years.
* Admitted to the study with a expected stay of more than 72 hours.
* Require initiation of enteral nutrition support.

Exclusion Criteria:

* Pre-existing severe gastrointestinal diseases.
* Patients with gastrointestinal bleeding.
* Patients with bowel obstruction.
* Pregnant or lactating women.
* Patients with contraindications to bedside Doppler ultrasound.

Where it's running

  • Peking union medical college hospital
    Beijing, Beijing Municipality, China
    Recruiting

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.