Aspiration pneumonia. Pneumonitis due to solids and liquids
Conditions
Interventions
Single group: Patients will receive a placebo for two months in the first phase, followed by probiotic administration for two months. The probiotic will be given as Perfect probiotic drops for childre
Sponsors
Tehran University of Medical Sciences
Eligibility
Sex/Gender
All
Age
4 Years to 8 Years
Inclusion criteria
Inclusion criteria: Children aged 4 to 8 years hospitalized due to aspiration pneumonia with cerebral palsy Parental consent for the child's participation in the study
Exclusion criteria
Exclusion criteria: onsumption of other related supplements, including probiotics and prebiotics Having an underlying related medical condition that affects the dependent variables, including physical and mental disabilities
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Sleep quality. Timepoint: Two months after placebo and two months after the main intervention. Method of measurement: General Children's Sleep Questionnaire. | — |
Secondary
| Measure | Time frame |
|---|---|
| Number of hospitalizations. Timepoint: Two months after giving the placebo and two months after the main intervention. Method of measurement: Based on the hospitalization record. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactFarshad Shabani
Tehran University of Medical Sciences
Outcome results
None listed