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Not yet recruitingNCT07888049Updated Oct 22, 2026

Neutrophil Monocyte Lymphocyte Ratios in Pediatric Chest Infections

An observational study in Pneumonia and Bronchiolitis, sponsored by Assiut University. Not yet recruiting. Open to participants aged 1 Month to 12 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-10-22.

Sponsored by Assiut University · Observational

Updated Oct 22, 2026Newly registeredGo to Updates ↓
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
120
Ages
1 Month to 12 Years
Sex
All
01

Study summary

This prospective cohort study aims to evaluate neutrophil-to-lymphocyte ratio, monocyte-to-lymphocyte ratio, and neutrophil-to-monocyte ratio in children with lobar pneumonia, bronchiolitis, and bronchopneumonia compared with healthy children.

Read the detailed description

Chest infections are a leading cause of pediatric morbidity. Complete blood count-derived inflammatory ratios such as neutrophil-to-lymphocyte ratio, monocyte-to-lymphocyte ratio, and neutrophil-to-monocyte ratio are simple and inexpensive parameters that may help in the assessment of children with respiratory infections.

This observational study will include four groups of children aged 1 month to 12 years: healthy controls, lobar pneumonia, bronchiolitis, and bronchopneumonia. Neutrophil-to-lymphocyte ratio, monocyte-to-lymphocyte ratio, and neutrophil-to-monocyte ratio will be calculated from complete blood count at admission.

02

Conditions studied

  • Pneumonia
  • Bronchiolitis

Keywords

  • Neutrophil-to-lymphocyte ratio
  • Monocyte-to-lymphocyte ratio
  • Pediatric chest infection
  • Pneumonia
  • Assiut
03

In context

Pneumonia

2,072 studies on the registry are indexed under Pneumonia; 286 are open to participants now.

This study's planned enrollment of 120 is below the median of 200 across 699 observational studies indexed under Pneumonia.

Browse Pneumonia 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 12 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Children aged 1 month to 12 years with lobar pneumonia, bronchiolitis, or bronchopneumonia, and healthy children of similar age, presenting to 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 12 years
  • Clinical diagnosis of lobar pneumonia, bronchiolitis, or bronchopneumonia (for disease groups)
  • Healthy children without acute illness (for control group)
  • Written informed consent from parent or legal guardian

Exclusion criteria

Exclusion Criteria:

  • - Age less than 1 month or greater than 12 years
  • Hospital-acquired infection
  • Immunodeficiency
  • Congenital heart disease
  • Chronic lung disease
  • Systemic steroid use during the preceding 2 weeks
  • Death within the first 24 hours
05

Study design

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

Groups and cohorts

  • Healthy Children

    Healthy children without acute respiratory illness serving as controls.

  • Lobar Pneumonia

    Children with clinical and radiographic findings of lobar pneumonia.

  • Bronchiolitis

    Children younger than 2 years with clinical diagnosis of bronchiolitis.

  • Bronchopneumonia

    Children with clinical and radiographic findings of bronchopneumonia.

06

What researchers measure

Primary outcomes

  1. Neutrophil-to-lymphocyte ratio

    Mean neutrophil-to-lymphocyte ratio calculated as absolute neutrophil count divided by absolute lymphocyte count.

    Time frame: Baseline

Secondary outcomes

  1. Monocyte-to-lymphocyte ratio

    Mean monocyte-to-lymphocyte ratio calculated as absolute monocyte count divided by absolute lymphocyte count.

    Time frame: Baseline

  2. Neutrophil-to-monocyte ratio

    Mean neutrophil-to-monocyte ratio calculated as absolute neutrophil count divided by absolute monocyte count.

    Time frame: Baseline

  3. Number of children requiring oxygen

    Number of children who require supplemental oxygen during hospital stay.

    Time frame: At 14 days

  4. Length of hospital stay

    Mean length of hospital stay in days.

    Time frame: At 14 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 272 non-industry observational studies under Pneumonia, half reached primary completion within 25 months of starting (the median), counting those still running; a quarter within 13 and three quarters within 56. This study's planned 12 months is below that.

Counting every sponsor, half of 281 studies reached it within 25 months; a quarter within 14 and three quarters within 53.

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

Registered
Oct 15, 2026
First posted
Oct 22, 2026
StartEst.
Oct 20, 2026
Primary completionEst.
Oct 20, 2027
CompletionEst.
Mar 20, 2028
Last update
Oct 22, 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 22, 2026
Show all 1 update
  1. Oct 22, 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
NCT07888049
Lead sponsor
Assiut University
Responsible party
Rania Ashraf Gaber Abdelghany (Resident Physician, Department of Pediatrics, Assiut University) — Principal investigator
First posted
Oct 22, 2026
Start date
Oct 20, 2026 (estimated)
Primary completion
Oct 20, 2027 (estimated)
Completion
Mar 20, 2028 (estimated)
Last update
Oct 22, 2026

Study contacts

Rania A Gaber, Resident
Contact
raniaashraf111997@gmail.com
+20 10 67454245
Mohamed H Ghazaly, 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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