Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
PHASE2
180 participants
INTERVENTIONAL
2023-01-05
2023-07-30
Brief Summary
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Therefore, based on data in the literature, it is understood that there is evidence of the effectiveness of using probiotics, either alone or in the form of a blend, to alleviate the symptoms of infantile colic.
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Detailed Description
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Parents and caregivers often seek medical attention for colic, including the use of medication, plant fiber, lactase, sucrose solution, hypoallergenic diet, and herbal tea. However, there is no single effective and safe intervention for infantile colic.
Interest in the use of probiotics as a potential treatment to reduce crying in babies with colic has increased lately. Recent studies have reported that the gut microbiota in infants with colic is characterized by lower proportions of Lactobacilli and Bifidobacteria and higher proportions of opportunistic proteobacteria (such as Escherichia coli, Enterobacter aerogenes and Klebsiella spp.) in comparison with the control babies. Thus, several researchers have suggested that probiotics may be useful in treating breastfed babies with colic and reducing crying time.
One study showed that administration of Lactobacillus reuteri DSM 17938 improved colic symptoms, although the effectiveness was only seen in breastfed and not formula fed infants. Another study showed that treatment with a combination of L. casei, L. rhamnosus, Streptococcus thermophilus, B. breve, L. acidophilus, B. infantiles, L. bulgaricus and fructooligosaccharides (FOS) reduced the duration of crying by almost 35 min compared to placebo. Furthermore, other authors has reported a reduced incidence of caregiver-reported colic when infants were supplemented with a combination of B. animalis subsp. lactis BB-12 and an unidentified strain of S. thermophilus, although colic was not formally diagnosed by a physician, which reduced the strength of the studies. A recent study on the same BB-12 strain overcame this deficiency by formally diagnosing colic using Rome-III criteria. However, this study showed that the response rate did not significantly improve over placebo until day 21. On the other hand, one study reported that the use of L. rhamnosus GG (ATCC53103) had no significant effect on crying in babies with colic. In another study, no significant differences were found in crying and irritability between the probiotic and placebo groups when supplemented with L. reuteri ATCC55730 or B. lactis BB-12.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
QUADRUPLE
Study Groups
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Placebo
product vehicle (sunflower oil)
Placebo
product vehicle (sunflower oil)
Limosilactobacillus reuteri CCT 7862
Limosilactobacillus reuteri CCT 7862 - 1 x 10e9 UFC/ daY.
Limosilactobacillus reuteri CCT 7862
Limosilactobacillus reuteri CCT 7862 - 1 x 10e9 UFC/ day.
Bifidobacterium lactis CCT 7858 + Lactobacillus rhamnosus CCT 7863
Blend: Bifidobacterium lactis CCT 7858 + Lactobacillus rhamnosus CCT 7863 - 1 x 10e9 UFC/ day.
Bifidobacterium lactis CCT 7858 + Lactobacillus rhamnosus CCT 7863
Bifidobacterium lactis CCT 7858 + Lactobacillus rhamnosus CCT 7863 - 1 x 10e9 UFC/ day
Interventions
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Placebo
product vehicle (sunflower oil)
Limosilactobacillus reuteri CCT 7862
Limosilactobacillus reuteri CCT 7862 - 1 x 10e9 UFC/ day.
Bifidobacterium lactis CCT 7858 + Lactobacillus rhamnosus CCT 7863
Bifidobacterium lactis CCT 7858 + Lactobacillus rhamnosus CCT 7863 - 1 x 10e9 UFC/ day
Eligibility Criteria
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Inclusion Criteria
* Informed consent form signed by parents
* Both gender
* Availability to complete scales daily and answer phone calls and/or text messages.
Exclusion Criteria
* current intake of antibiotics, prebiotics, or probiotics by the baby or mother;
* Children with known moderate or severe disease of any system (neural, skeletal, muscular, cutaneous, gastrointestinal, respiratory, genital, urinary, immune),
* parental difficulty in understanding study requirements as judged by physician.
17 Days
23 Days
ALL
Yes
Sponsors
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Universidade do Extremo Sul Catarinense - Unidade Academica de Ciecias da Saude
OTHER
Responsible Party
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Monique Michels
Principal Investigator
Locations
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Monique Michels
Criciúma, Santa Catarina, Brazil
Countries
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Facility Contacts
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Other Identifiers
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63543922.2.0000.0119
Identifier Type: -
Identifier Source: org_study_id
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