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Efficacy of Lactobacillus Reuteri DSM 17938 for the Treatment of Acute Gastroenteritis in Children

Efficacy of Lactobacillus Reuteri DSM 17938 for the Treatment of Acute Gastroenteritis in Children: Randomised Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02989350
Enrollment
100
Registered
2016-12-12
Start date
2017-01-16
Completion date
2018-11-30
Last updated
2019-01-30

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

Conditions

Acute Gastroenteritis

Brief summary

Acute gastroenteritis (AGE) is one of the most common diseases among children. Oral rehydration therapy is the key treatment. According to the 2014 guidelines developed by the ESPGHAN probiotics may be considered in the management of children with AGE in addition to rehydration therapy. Considering that evidence on L reuteri remains limited, the investigators aim to assess the efficacy of L reuteri DSM 17938 for the treatment of AGE in children. Children vaccinated and not vaccinated against rotavirus will be evaluated separately. Two independent reports (rotavirus-vaccinated and non-vaccinated children) are planned.

Interventions

Lactobacillus reuteri DSM 17938 vs Placebo

DIETARY_SUPPLEMENTPlacebo

Lactobacillus reuteri DSM 17938 vs Placebo

Sponsors

Szpital im. Św. Jadwigi Śląskiej
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
2 Months to 60 Months
Healthy volunteers
No

Inclusion criteria

1. Acute gastroenteritis (AGE) defined as a change in stool consistency to loose or liquid form (according to the Bristol Stool Form (BSF) scale or in the case of infants, the Amsterdam Stool Form (ASF) scale) and/or an increase in the frequency of evacuations (typically ≥3 in 24 h), lasting for no longer than 5 days. 2. Age: older than 1 month and younger than 60 months. 3. A caregiver must provide written informed consent.

Exclusion criteria

1. Use of antibiotics within two weeks prior to enrolment. 2. Use of gelatine tannate, diosmectite, probiotics, racecadotril, or zinc (including zinc containing ORS) within a week prior to enrolment (a single dose is allowed). 3. Breast feeding (\>50%) 4. Chronic diarrhoeal gastrointestinal disease (e.g., inflammatory bowel disease, cystic fibrosis, coeliac disease, food allergy) 5. Immunodeficiency 6. Malnutrition (weight/height/length under 3rd percentile) (WHO Child Growth Standards will be used)

Design outcomes

Primary

MeasureTime frameDescription
Duration of diarrhea8 days(measured in hours) - time until the normalisation of stool consistency according to the Bristol Stool Form Scale(BSF) or Amsterdam Infant Stool Scale (ASF) - (in BSF scale, numbers 1, 2, 3, 4 and 5; in ASF scale, letters B or C), or the time until the normalisation of the number of stools (compared with the period before the onset of diarrhoea).and the presence of normal stools for 48 h.

Secondary

MeasureTime frameDescription
Duration of intravenous rehydration8 days
Need for hospitalisation of outpatients8 daysNumber of patients enrolled as outpatient requiring hospitalisation - based on medical assesment
Number of watery stools per day8 days
Vomiting8 daysNumber of participants with vomits and number of vomits per day
Need for intravenous rehydration8 daysNumber of patients in each group requiring intravenous rehydration
Severity of diarrhoea according to Vesikari scale8 days
Use of concomitant medications8 days
Adverse events8 days
Recurrence of diarrhoea (in 48 hours after intervention)48 hoursNumber of patients in which diarrhoea recur after initial recovery in 48 hours

Countries

Poland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 26, 2026