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Completed

NCT Number: NCT06005454

The Impact of Fish Oil Supplementation on the Outcome of Children with Pneumonia I

The aim of study is to investigate the effect of enteral feeding of Omega-3 on the outcome of children with Pneumonia in PICU

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Key information

Age range

1 month–5 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Hoda Atef Abdelsattar Ibrahim

Cairo, Egypt

About this study

Group A(cases) will be supplemented by omega-3 fatty acids for immediate post admission consecutive 7 days besides conventional treatment of pneumonia, in a dose of 350 mg twice daily for children less than 3 years and 450 mg twice daily for older children according to the standard treatment per the American Institute of Medicine of the National Academies guidelines for maximum dose for this age group. (Institute of Medicine of the National Academies,2016)

Side effects of omega-3 supplements are usually mild. They include unpleasant taste, bad breath, bad-smelling sweat, headache, and gastrointestinal symptoms such as heartburn, nausea, and diarrhea. (Office of Dietary Supplements ,2016)

Group B(controls) will be received enteral feeding without omega-3 fatty acid support.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • All children patients with severe pneumonia admitted to PICU
  • Both sexes
  • Age: under 5 years
  • Whose parents or caregivers approve for participation in the study

Exclusion criteria

  • Patients with chronic illnesses to exclude bias that could be emerged due to the chronic disease effect
  • Whose parents or caregivers will not apply for participation in the study
  • Patients who will be contraindicated for enteral feeding

Treatment and study plan

Fish oil (Omega)

Dietary Supplement

We will use a dietary supplement source of omega 3 fatty acids from the available syrup ( each 5 ml contain 640 mg of high DHA Fish oil) so we will give it in a dose 2.7 ml twice daily for children between 1 and 3 years and 3.5 ml twice daily for children between 4 and 5 years.

Primary outcomes

  1. Hospital length stay

    Time frame: Through study completion, an average of 1 yea

    Hospital length stay will be measured between the two groups

Sponsors and collaborators

Lead sponsor

Cairo University

Other

Registry information

Official study title

The Impact of Fish Oil Supplementation on the Outcome of Children with Pneumonia in the Intensive Care Unit

Important dates

Study start
2023
Primary completion
2024
Study completion
2024
First posted
Aug 22, 2023
Registry last updated
Mar 19, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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