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    Genovis Inc prospective randomisation
    Prospective Randomisation, supplied by Genovis Inc, used in various techniques. Bioz Stars score: 99/100, based on 14462 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Average 99 stars, based on 14462 article reviews
    prospective randomisation - by Bioz Stars, 2026-04
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    Figure 2 | Percentage of patients with persisting watery diarrhoea in the groups receiving placebo (grey) and Lactobacillus reuteri (white).

    Journal: Alimentary pharmacology & therapeutics

    Article Title: Randomised clinical trial: Lactobacillus reuteri DSM 17938 vs. placebo in children with acute diarrhoea--a double-blind study.

    doi: 10.1111/j.1365-2036.2012.05180.x

    Figure Lengend Snippet: Figure 2 | Percentage of patients with persisting watery diarrhoea in the groups receiving placebo (grey) and Lactobacillus reuteri (white).

    Article Snippet: Diarrhoea typically lasts less than 7 days and not longer than 14 days.1 The incidence of acute diarrhoea ranges from 0.5 to 1.9 episodes per child per year in children younger than 3 years old in Europe, with Rotavirus being the most frequent agent.1 Oral rehydration therapies (ORT) are the mainstay of management of acute diarrhoea.1, 2 Although its composition continues to improve, the oral glucose-electrolyte rehydration solution (ORS) recommended by the European Society of Paediatric Gastroenterology, Hepatology and Nutrition (ESPGHAN) and United Nations Children’s Fund neither shortens the duration of the illness nor reduces the stool loss and may in fact increase the stool volume at least during the first hours in children with acute diarrhoea.3 Probiotics may be an effective adjunct to the management of acute diarrhoea and a recent meta-analysis has shown that used alongside rehydration therapy, probiotics appear to be safe and have clear beneficial effects in shortening the duration and reducing stool frequency in acute infectious diarrhoea.4 However, more research is needed to guide the use of particular probiotic regimens and strain1, 2, 4 and as there is still no evidence of efficacy for many preparations, the ESPGHAN and the National Institute for Health and Clinical Excellence have suggested the use of probiotic strains with proven efficacy and in appropriate doses for the management of children with acute gastroenteritis as an adjunct to rehydration therapy.1, 2 Previously, in two separate prospective randomised trials Lactobacillus reuteri (L. reuteri) ATCC 55730 was shown to effectively colonise the gastrointestinal tract and to significantly shorten the duration of watery diarrhoea associated with rotavirus infection.5, 6 Recently, this strain was found to carry specific, unusual, potentially transferable resistance traits for tetracycline and lincomycin, which led to the development of a new daughter strain, L. reuteri DSM 17938 derived from L. reuteri ATCC 55730 by the natural removal of these unwanted plasmid-borne resistances.7 The daughter strain retained the probiotic properties and its safety and tolerance in adults.7 The aim of the present study was to assess the efficacy of this new strain of L. reuteri DSM 17938 as an adjunct to rehydration therapy in the treatment of children hospitalised with acute diarrhoea.

    Techniques: