Study on the evaluation of enteral nutrition implementation in shock patients by gastrointestinal ultrasound combined with biochemical indicators of intestinal barrier

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2300076077

Enrollment

Unknown

Registered

2023-09-25

Start date

2023-09-25

Completion date

Unknown

Last updated

2023-10-03

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

Conditions

SHOCK

Interventions

Case series:NA

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Shock patients with stable hemodynamics (when the dosage of vasoactive drugs is stable or reduced, and norepinephrine is = 0.5ug/kg/min) plan to initiate enteral nutrition; 2. Age 18 years or older; 3. Stay in ICU for more than 24 hours, NRS-2002 = 3; 4. Signed informed consent form.

Exclusion criteria

Exclusion criteria: 1. There are contraindications for enteral nutrition (uncontrolled shock, uncontrolled hypoxemia and acidosis, active gastrointestinal bleeding, intestinal ischemia and obstruction, abdominal compartment syndrome, high flow intestinal fistula without distal feeding channels); 2. Previous chronic gastrointestinal diseases (such as Crohn's disease, ulcerative colitis) or admission to the ICU due to abdominal surgery; 3. Chronic severe liver disease, chronic renal failure, advanced tumors; 4. Pregnancy or lactation; 5. Multiple organ failure, brain death.

Design outcomes

Primary

Measure	Time frame
Gastrointestinal ultrasound;Mesenteric circulation hemodynamics;	—

Secondary

Measure	Time frame
Biochemical indicators of intestinal barrier;	—

Countries

China

Contacts

Public ContactShen Ji

Jiangyin People's Hospital

irwiner1@sina.com+86 188 6171 1509

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026