Evaluation of Enteral Nutrition in Critically Ill Children

NCT04013893 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 20

Last updated 2019-07-12

No results posted yet for this study

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.

Conditions

  • Critical Illness
  • Enteral Feeding Intolerance

Sponsors & Collaborators

  • Cukurova University

    lead OTHER

Principal Investigators

  • Dincer Yildizdaş, Professor · Cukurova University Medicine Faculty

Eligibility

Min Age
1 Month
Max Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-06-01
Primary Completion
2020-01-01
Completion
2020-06-01

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04013893 on ClinicalTrials.gov