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Yogurt Probiotic Bacteria on Relieving Young Children Acute Gastroenteritis

Effect of Mothers' Application of Yogurt Probiotic Bacteria on Relieving Their Young Children's Acute Gastroenteritis

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06090708
Enrollment
60
Registered
2023-10-19
Start date
2022-11-01
Completion date
2023-07-27
Last updated
2023-10-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Gastroenteritis

Keywords

Yogurt Probiotic Bacteria, young Children, Gastroenteritis

Brief summary

The goal of this clinical trial is to test the effect of mothers' application of yogurt probiotic bacteria on relieving their young children's acute gastroenteritis in children had two to five years old. The main hypothesis is children with acute gastroenteritis who receive yogurt probiotic bacteria exhibit less diarrhea, vomiting and dehydration than those who don't.The study subjects were divided into two equal groups (probiotic study group and control group).

Interventions

DIETARY_SUPPLEMENTyogurt with probiotic bacteria

Children in probiotic study group were received 15 mg/kg of market available fresh probiotic yogurt after stopping vomiting every four to six hours for three consecutive days beside to the standard hospital care and the prescribed medication for acute gastroenteritis.

Sponsors

Alexandria University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
1 Years to 5 Years
Healthy volunteers
Yes

Inclusion criteria

* newly admitted children with no or some dehydration and with acute gastroenteritis.

Exclusion criteria

* bloody watery diarrhea

Design outcomes

Primary

MeasureTime frameDescription
Skin pinchbefore intervention, after 1st day of study, after 2nd day of study, and after 3rd day of study.Goes back quickly/ Goes back slowly/ Goes back very slowly
Amount of Vomitingbefore intervention, after 1st day of study, after 2nd day of study, and after 3rd day of study.Small / moderate/ large/ severe
Frequency of Vomitingbefore intervention, after 1st day of study, after 2nd day of study, and after 3rd day of study.times /day.
Consistency of Vomitingbefore intervention, after 1st day of study, after 2nd day of study, and after 3rd day of study.Soft/ watery/ abnormal constitute
Duration of Vomitingbefore intervention, after 1st day of study, after 2nd day of study, and after 3rd day of study./days.
General condition of childbefore intervention, after 1st day of study, after 2nd day of study, and after 3rd day of study.Normal/ Restless, irritable/ Lethargic or unconscious
Eyebefore intervention, after 1st day of study, after 2nd day of study, and after 3rd day of study.Normal/ Sunken eyes/ Very Sunken eyes
Thirstybefore intervention, after 1st day of study, after 2nd day of study, and after 3rd day of study.Drink normally/ Drinks eagerly, thirsty/ Drinks poorly or unable to drink
Experience of diarrheabefore intervention, after 1st day of study, after 2nd day of study, and after 3rd day of study.yes/no
Consistency of diarrheabefore intervention, after 1st day of study, after 2nd day of study, and after 3rd day of study.Soft/ watery/ abnormal constitute
Amount of diarrheabefore intervention, after 1st day of study, after 2nd day of study, and after 3rd day of study.Small / moderate/ large/ severe
Frequency of diarrheabefore intervention, after 1st day of study, after 2nd day of study, and after 3rd day of study.times /day.
Odor of diarrheabefore intervention, after 1st day of study, after 2nd day of study, and after 3rd day of study.No odor/ offensive odor
Duration of diarrheabefore intervention, after 1st day of study, after 2nd day of study, and after 3rd day of study./days.
Experience of Vomitingbefore intervention, after 1st day of study, after 2nd day of study, and after 3rd day of study.Yes/ no

Other

MeasureTime frameDescription
gender/before data collectionmale, female
residence/before data collectionurban,rural
type of feedingbefore data collectionbreast feeding, bottle feeding, mixed type, ordinary
diagnosisbefore data collectiongastroenteritis, bronchitis
prescribed medicationbefore data collectionantiemetics, fluids therapy, antibiotics
children's weightbefore data collection/kgs
children's age/before data collectionyear(s)

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 6, 2026