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Not yet recruitingNCT07884838Updated Oct 21, 2026

Enteral Feeding in Mechanically Ventilated Children

An observational study in Critical Illness and Mechanical Ventilation Complication, sponsored by Assiut University. Not yet recruiting. Open to participants aged 1 Month to 18 Years. Per ClinicalTrials.gov, last updated 2026-10-21.

Sponsored by Assiut University · Observational

Updated Oct 21, 2026Newly registeredGo to Updates ↓
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
60
Ages
1 Month to 18 Years
Sex
All
01

Study summary

This prospective cohort study aims to assess enteral feeding practices and the adequacy of energy and protein delivery among mechanically ventilated children admitted to the pediatric intensive care unit.

Read the detailed description

Children requiring invasive mechanical ventilation in the pediatric intensive care unit are at high risk of inadequate energy and protein intake. Enteral nutrition is preferred when the gastrointestinal tract is functional.

This observational study will prospectively evaluate the timing of initiation, adequacy of energy and protein delivery, feeding interruptions, and selected clinical outcomes in mechanically ventilated children admitted to the PICU at Assiut University Children's Hospital.

02

Conditions studied

  • Critical Illness
  • Mechanical Ventilation Complication

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Keywords

  • Enteral nutrition
  • Nutritional adequacy
  • Pediatric intensive care
  • Mechanical ventilation
  • Assiut
03

In context

Critical Illness

1,923 studies on the registry are indexed under Critical Illness; 465 are open to participants now.

This study's planned enrollment of 60 is below the median of 130 across 883 observational studies indexed under Critical Illness.

Browse Critical Illness studies →

Lead sponsor

Assiut University is the lead sponsor of 5,050 studies on the registry; 2,174 are open to participants now.

Of its 14 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
1 Month to 18 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Mechanically ventilated children aged 1 month to 18 years admitted to the Pediatric Intensive Care Unit of Assiut University Children's Hospital.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • - Children aged 1 month to 18 years
  • Admission to the PICU
  • Requirement for invasive mechanical ventilation
  • Expected PICU stay sufficient for assessment of nutritional delivery
  • Written informed consent from parent or legal guardian

Exclusion criteria

Exclusion Criteria:

  • - Neonates under 1 month of age
  • Absolute contraindication to enteral feeding
  • Exclusive parenteral nutrition from admission
  • Death or transfer within 48 hours of admission
  • Inborn errors of metabolism needing special diets
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
60 participants (estimated)
Patient registry
No

Groups and cohorts

  • Mechanically Ventilated Children

    Children aged 1 month to 18 years requiring invasive mechanical ventilation in the PICU who will be followed for enteral feeding practices and nutritional adequacy.

06

What researchers measure

Primary outcomes

  1. Number of children achieving adequate energy delivery

    Number of mechanically ventilated children who achieve predefined adequate energy delivery during the assessment period.

    Time frame: At 7 days

Secondary outcomes

  1. Energy adequacy percentage

    Mean energy adequacy calculated as actual energy received divided by estimated energy requirement multiplied by 100.

    Time frame: At 7 days

  2. Time to initiation of enteral feeding

    Mean time in hours from PICU admission to initiation of enteral feeding.

    Time frame: At 7 days

  3. Duration of mechanical ventilation

    Mean duration of invasive mechanical ventilation in days.

    Time frame: At 28 days

  4. PICU length of stay

    Mean length of stay in the pediatric intensive care unit in days.

    Time frame: At 28 days

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Start is estimated for Oct 2026; primary completion for Oct 2027, 12 months later.

Of 473 non-industry observational studies under Critical Illness, half reached primary completion within 22 months of starting (the median), counting those still running; a quarter within 11 and three quarters within 43. This study's planned 12 months is below that.

Counting every sponsor, half of 477 studies reached it within 22 months; a quarter within 11 and three quarters within 43.

Critical Illness covers many different conditions, not one, so the studies compared here vary widely. Read these figures as a rough guide.

How these figures are worked out, and which studies are left out of them.

Registered
Oct 14, 2026
First posted
Oct 21, 2026
StartEst.
Oct 26, 2026
Primary completionEst.
Oct 26, 2027
CompletionEst.
Feb 10, 2028
Last update
Oct 21, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Registered
First appeared on the registry. No changes since
Oct 21, 2026
Show all 1 update
  1. Oct 21, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07884838
Lead sponsor
Assiut University
Responsible party
Marina Helal Marzouk Badros (Resident Physician, Department of Pediatrics, Assiut University) — Principal investigator
First posted
Oct 21, 2026
Start date
Oct 26, 2026 (estimated)
Primary completion
Oct 26, 2027 (estimated)
Completion
Feb 10, 2028 (estimated)
Last update
Oct 21, 2026

Study contacts

Marina H Marzouk, Resident
Contact
marinahelal33@gmail.com
+20 12 11834760
Ismail L Mohammed, prof
study chair · Pediatrics Department, Assiut University Hospitals

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.

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Discussion

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