Skip to content

Development and validation of a nomogram for predicting feeding intolerance in critically ill patients

Development and validation of a nomogram for predicting feeding intolerance in critically ill patients

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300071370
Enrollment
Unknown
Registered
2023-05-12
Start date
2023-05-30
Completion date
Unknown
Last updated
2023-06-12

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

Conditions

Feeding intolerance in severe cases

Interventions

Case series:None

Sponsors

The First Hospital of Jilin University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: (1) Age =18 years old; (2) Start EN within 48 hours after ICU admission; (3) Continuous feeding with continuous infusion, short peptide preparation or whole protein preparation;(4)Has signed informed consent (only for the second stage).

Exclusion criteria

Exclusion criteria: (1) Meet the 2012 AGI Level IV diagnostic criteria of ESICM within 24 hours after admission to ICU (gastrointestinal failure with effects on distant organ function); (2) combined oral ingestion during the first 7 days of ICU; (3)Patients who have applied EN within 3 days prior to admission to the ICU; (4)Patients with cross-use of EN preparations before feeding intolerance occurs; (5)Pregnant women; (6)Patients participating in other clinical studies; (7)Patients whose clinical data were missing (only for the first stage); (8)Patient requires withdrawal in the second stage (only for the second stage).

Design outcomes

Primary

MeasureTime frame
Feeding intolerance;

Countries

China

Contacts

Public ContactDong Zhang

The First Hospital of Jilin University

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

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 12, 2026