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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05900167
Other study ID # IIT-2023-0054
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date June 1, 2023
Est. completion date October 1, 2024

Study information

Verified date June 2023
Source RenJi Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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


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


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 442
Est. completion date October 1, 2024
Est. primary completion date October 1, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

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

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Xiao Jie Chen

Outcome

Type Measure Description Time frame Safety issue
Primary Feeding intolerance Any symptoms of gastrointestinal adverse reactions are defined as feeding intolerance 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
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