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Feeding Intolerance Risk Prediction Model in Patients With Enteral Nutrition Through Nasogastric Tube

Feeding Intolerance Risk Prediction Model in Patients With Enteral Nutrition Through Nasogastric Tube

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05900167
Enrollment
442
Registered
2023-06-12
Start date
2023-06-01
Completion date
2024-10-01
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

Enteral Nutrition

Brief summary

To explore the risk factors of enteral feeding intolerance in critically ill patients, build a risk prediction model and verify it, in order to provide reference for early identification and screening of high-risk groups

Detailed description

Based on the previous literature study, the risk factors of enteral feeding intolerance in critically ill patients were obtained, and the general demographic, disease and treatment information of patients were collected. Four machine learning algorithms, namely traditional logistic regression, random forest, support vector machine and naive Bayes, were used to construct risk prediction models, and the optimal model was selected and verified by comparing the model performance

Interventions

BEHAVIORALenteral nutrition

The nutritional status of the patient is assessed by the physician to determine the need for enteral nutrition

Sponsors

Xiao Jie Chen
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* The nutritional status of the patient is assessed by the doctor and the need for enteral nutrition is determined;Patients with first nasogastric tube insertion and successful enteral feeding;There was no gastrointestinal discomfort before enteral nutrition;Patients (or family members) authorized to participate in this study and signed informed consent

Exclusion criteria

* Previous gastrointestinal disease or gastrointestinal surgery;enteral nutrition through gastrostomy tube or jejunostomy tube;discontinuation or suspension of enteral nutrition for special reasons other than feeding intolerance;Patients with serious lack of clinical data

Design outcomes

Primary

MeasureTime frameDescription
Feeding intoleranceFollow-up was considered complete when the patient reached 7 days of enteral nutrition, the patient was transferred from the ICU, or the patient experienced nutritional interruption for other reasonsAny symptoms of gastrointestinal adverse reactions are defined as feeding intolerance

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026