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Clinical Trials/NCT04013893
NCT04013893
Unknown
Not Applicable

Evaluation of Enteral Nutrition in Critically Ill Children Receiving Inotropic Support in Pediatric Intensive Care Unit

Cukurova University1 site in 1 country20 target enrollmentJune 1, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Critical Illness
Sponsor
Cukurova University
Enrollment
20
Locations
1
Primary Endpoint
28-d mortality
Last Updated
6 years ago

Overview

Brief Summary

The aim of this study was to evaluate the effect of calorie and enteral feeding timing on survival in critically ill children receiving inotropic, vasopressor and inodilatory supplements.

Detailed Description

The aim of this study was to evaluate the effect of calorie and enteral feeding timing on survival in critically ill children receiving inotropic, vasopressor and inodilatory supplements. Early enteral nutrition will be initiated within the first 24 hours of hospitalization in critically ill children who have inotropic vasopressor and inodilator support without any problems and contraindications in gastrointestinal system functions. The energy requirement of the intubated patients will be measured by indirect calorie meter method. Schofield method will be used to calculate the daily energy needs of extubated patients. 30% of the targeted energy in the first 48 hours of hospitalization and 80% of the targeted energy in the first week will be achieved by enteral nutrition.Nutritional solutions with a concentrated formula of 1 / 1.5 will be given to patients with cardiac pulmonary or renal disease requiring fluid restriction.Patients will be followed up for vomiting, diarrhea, abdominal distention, feeding intolerance, gastric residues and gastrointestinal bleeding. If these findings develop, the patient's nutrition will be interrupted according to the clinician's assessment and enteral nutrition will be re-fed as soon as possible.

Registry
clinicaltrials.gov
Start Date
June 1, 2019
End Date
June 1, 2020
Last Updated
6 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Ahmet Yontem

Principal Investigator

Cukurova University

Eligibility Criteria

Inclusion Criteria

  • Children with normal gastrointestinal system function
  • Children receiving inotropic, vasopressor or inodilatory support

Exclusion Criteria

  • Children with gastrointestinal system dysfunction
  • Children with enteral nutrition contraindicated
  • Children with metabolic disease with special nutrition

Outcomes

Primary Outcomes

28-d mortality

Time Frame: 28 days

To evaluate the effect of enteral feeding timing on survival

Secondary Outcomes

  • Vasoactive inotrope score(During inotropic treatment)
  • Lactate(During inotropic treatment)

Study Sites (1)

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