Actively Recruiting
Correlation Study Between SMA Blood Flow Reactivity and Acute Gastrointestinal Functional Injury in Critically Ill Patients
Led by Peking Union Medical College Hospital · Updated on 2025-09-05
80
Participants Needed
1
Research Sites
4 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are examining how blood flow in the superior mesenteric artery (SMA) changes after feeding in critically ill patients in the intensive care unit (ICU). The study seeks to understand the connection between these blood flow changes and the risk of Acute Gastrointestinal Injury (AGI), aiming to develop a model that predicts AGI risk based on SMA blood flow reactivity. This research focuses on improving enteral nutrition safety and patient outcomes by tailoring feeding strategies using intestinal blood flow information. The study uses enteral nutrition with intact protein formulas delivered through a nasogastric tube, starting at a rate of 20 ml per hour for 24 hours. Feeding adjustments are made based on real-time monitoring of SMA blood flow using bedside Doppler ultrasound. This observational approach allows researchers to closely observe how intestinal blood flow responds to feeding and its relation to gastrointestinal function. Participants will be monitored from enrollment through at least three days of treatment, with assessments focusing on feeding intolerance and gastrointestinal status. Researchers will use ultrasound to track SMA blood flow changes and evaluate hemodynamic indicators. The study aims to identify patterns in blood flow that predict gastrointestinal injury, enhancing personalized nutrition plans. Overall participation will include these monitoring and feeding evaluations during the hospital stay.
CONDITIONS
Brief Title
Correlation Study Between SMA Blood Flow Reactivity and Acute Gastrointestinal Injury in Critically Ill Patients
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults aged 18 years and older up to 80 years
- Expected hospital stay longer than 72 hours
- Require initiation of enteral nutrition support
You will not qualify if you...
- Pre-existing severe gastrointestinal diseases
- Gastrointestinal bleeding
- Bowel obstruction
- Pregnant or lactating women
- Contraindications to bedside Doppler ultrasound
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 3 days
Participants are observed to assess SMA blood flow reactivity and gastrointestinal function while receiving enteral nutrition.
Continuous monitoring during enteral nutrition support
Trial Site Locations
Total: 1 location
1
Peking union medical college hospital
Beijing, Beijing Municipality, China, 100730
Actively Recruiting
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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