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An Investigation of the Interventional Effect of Using Probiotics and Zinc in the Treatment of Admitted Children with Bacterial Pneumonia

Phase 3
Conditions
Bacterial pneumonia.
Bacterial pneumonia, not elsewhere classified
Registration Number
IRCT20190611043869N1
Lead Sponsor
Sabzevar University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
135
Inclusion Criteria

Infants and children aged 1 months up to 18 years if diagnosed on medium to very severe bacterial pneumonia
Shift left-sided leukocytosis, or Erythrocyte Sedimentation Rate(ESR) and C- Reactive Protein(CRP), or pulmonary involvement in radiography (Basis of clinical, radiographic, and laboratory findings from the Integrated Management of Childhood Illness (IMCI) and Nelson 2016).

Exclusion Criteria

Cystic fibrosis, maternal coronary heart disease, immunodeficiency, chronic heart disease, developmental delay, and Failure to Thrive(FTT) (weight for age below the 3rd percentile).
Parental dissatisfaction

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Tachypnea. Timepoint: Daily during hospitalization. Method of measurement: Physical Examination.;Subcostal, Intercostal, Suprasternal Retraction. Timepoint: Daily during Hospitalization. Method of measurement: Physical Examination.;Nasal Flaring. Timepoint: Daily during hospitalization. Method of measurement: Physical Examination.;Temperature. Timepoint: Daily during Hospitalization. Method of measurement: Thermometer.;Respiration Rate. Timepoint: Daily during Hospitalization. Method of measurement: Cornometer.;Cough. Timepoint: Daily during hospitalization. Method of measurement: Physical Examination.;Crackle. Timepoint: Daily during hospitalization. Method of measurement: Physical Examination.;Wheezing. Timepoint: ??Daily during hospitalization. Method of measurement: Physical Examination.
Secondary Outcome Measures
NameTimeMethod
Diarrhea. Timepoint: Daily during hospitalization. Method of measurement: Observation.
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