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Modifying feeding protocols for critically ill patients (mNEED) based on a predictive model of feeding intolerance in critically ill patients: a multicentre, cluster randomized, controlled trial

Modifying feeding protocols for critically ill patients (mNEED) based on a predictive model of feeding intolerance in critically ill patients: a multicentre, cluster randomized, controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400081581
Enrollment
Unknown
Registered
2024-03-05
Start date
2024-10-01
Completion date
Unknown
Last updated
2024-03-11

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

Conditions

Critically ill patient

Interventions

mNEED Group :Nutritional interventions were implemented in accordance with mNEED feeding regimen developed by us
NEED Group :Nutritional interventions were implemented in accordance with the NEED feeding programme proposed in 2022

Sponsors

Tthe First Hospital of Jilin University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: (1) Age 18 or older; Failure of one or more organ systems within 24 hours of admission to the ICU (Sequential Organ Failure Assessment (SOFA) score =2 for any single organ system); (3) Expected stay in ICU for more than 48 hours ICU inclusion criteria: (1) ICU in level 2 and above hospitals; (2) ICU with the ability to carry out intensive care and monitor patient FI; (3) The type of ICU was emergency, medical, surgical, neurosurgical, or comprehensive ICU

Exclusion criteria

Exclusion criteria: (1) Patients have received EN treatment in the past three days; (2) Is receiving palliative care and is expected to die within 48 hours; (3) Pregnancy; (4) Long-term use of steroids or other immunosuppressants; (5) Patients undergoing radiotherapy or chemotherapy for malignant diseases; (6) Participate in other clinical studies ICU exclusion criteria: (1) ICU that refused to participate in the study; (2) ICU that has not passed the ethical review;

Design outcomes

Primary

MeasureTime frame
Feeding intolerance;

Secondary

MeasureTime frame
Nutrient supply compliance rate;Mortality rate at 28 and 90 days ;Length of ICU stay;

Countries

China

Contacts

Public ContactDong Zhang

First Hospital of Jilin University

zhangdong@jlu.edu.cn+86 159 4835 0236

Outcome results

None listed

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