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Evidence-Based Supplement Research
Evidence-Based Supplement Research

Lack of Benefit of Lactobacillus reuteri DSM 17938 as an Addition to the Treatment of Functional Constipation.

  • 2018-12
  • Journal of pediatric gastroenterology and nutrition 67(6)
    • Oleg Jadrešin
    • Sara Sila
    • Ivana Trivić
    • Zrinjka Mišak
    • Iva Hojsak
    • Sanja Kolaček

Study Design

Type
Randomized Controlled Trial (RCT)
Sample size
n = 33
Population
33 children (12 girls, median age 4.5 years, range 2-16)
Methods
single-center randomized, double-blind, placebo-controlled study; intervention group received L reuteri DSM 17983 and lactulose, placebo group received placebo and lactulose
Blinding
Double-blind
Funding
Unclear
The aim of this study was to investigate the role of Lactobacillus reuteri DSM 17983 in the treatment of functional constipation in children. The trial was a single-center randomized, double-blind, placebo-controlled study. Patients were allocated into the 2 groups; intervention group which received L reuteri DSM 17983 and lactulose and placebo group which received placebo and lactulose. Due to small recruitment rate study was terminated prematurely; therefore, only 33 children (12 girls, median age 4.5 years, range 2-16) were randomized. There was no difference between groups in the stool frequency, stool consistency, pain, soiling rate and dose of the lactulose. This study found that L reuteri DSM 17938 adds no benefit to the treatment of constipation in children. Due to small sample size, these results, however, should be interpreted with caution.

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