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Clinical Trials/NCT05900167
NCT05900167
Not yet recruiting
Not Applicable

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

Xiao Jie Chen0 sites442 target enrollmentStarted: June 1, 2023Last updated:

Overview

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Xiao Jie Chen
Enrollment
442
Primary Endpoint
Feeding intolerance

Overview

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

Study Design

Study Type
Observational
Observational Model
Other
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts 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

Outcomes

Primary Outcomes

Feeding intolerance

Time Frame: Follow-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 reasons

Any symptoms of gastrointestinal adverse reactions are defined as feeding intolerance

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Xiao Jie Chen
Sponsor Class
Other
Responsible Party
Sponsor Investigator
Principal Investigator

Xiao Jie Chen

Nurse

RenJi Hospital

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