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Study the effects of probiotics in the prevention of antibiotic-associated diarrhea in children

Study the effects of probiotics in the prevention of antibiotic-associated diarrhea in children

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201205229828N1
Enrollment
230
Registered
2012-07-09
Start date
2010-06-22
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Diarrhea. Other gastroenteritis and colitis of infectious and unspecified origin

Interventions

Intervention 1: The intervention group receiving Probiotic packages As a daily Prvtksyn Sasht To ten days .Probiotics contain a billion or a phrase such as Sasht 10*9 live microorganisms that are cons
Treatment - Drugs
Placebo
The intervention group receiving Probiotic packages As a daily Prvtksyn Sasht To ten days .Probiotics contain a billion or a phrase such as Sasht 10*9 live microorganisms that are considered for each
The control group received a placebo that are quite similar with probiotic. The control group receiving Placebo packages As a daily Prvtksyn Sasht To ten days .Placebo are considered for each patient

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 14 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria : Children 6 months to 14 years ; Due to upper respiratory infection or ear infection ; Referred to in the first 24 hours of starting antibiotics Exclusion criteria: Severe infection or bacterial genaralyze ; Antibiotic treatment within 2 months before treatment ; Antibiotic prophylaxis; The use of probiotic products in recent months;Known immunodeficiency; Chronic intestinal infection; Acute and chronic diarrhea; Use more than one type of antibiotic treatment during the period; Heart or lung disease or severe renal, Lactase deficiency is known; viral gastroenteritis (rotavirus) ; Passing blood in the stool,Vomiting with diarrhea and severe dehydration;Incorrect or incomplete use of antibiotics ; failure to complete treatment course

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Diarrhea. Timepoint: Over a period of more than three loose stools in 48 hours. Method of measurement: Question of the mother.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSimin Partovi

Ghaem Hospital

partovis@mums.ac.ir+98 51 1840 0001

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026