Probiotics Strains for Infant Colic

NCT ID: NCT05685030

Last Updated: 2023-01-13

Study Results

Results pending

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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Recruitment Status

UNKNOWN

Clinical Phase

PHASE2

Total Enrollment

180 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-01-05

Study Completion Date

2023-07-30

Brief Summary

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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.

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.

Detailed Description

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Infantile colic represents a self-limiting temporary condition, which occurs in about one in five babies in the first few months of life, and is characterized by inconsolable crying and fussiness of unknown cause. Despite its benign nature, infantile colic serves as a significant source of maternal anxiety and depression, impaired family functioning, and the most common reason for seeking medical advice in this age group. Infant colic is also associated with sleep problems in babies.

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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Colic

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Phase II randomized, placebo-controlled, triple-blind clinical trial.
Primary Study Purpose

PREVENTION

Blinding Strategy

QUADRUPLE

Participants Caregivers Investigators Outcome Assessors

Study Groups

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Placebo

product vehicle (sunflower oil)

Group Type PLACEBO_COMPARATOR

Placebo

Intervention Type DIETARY_SUPPLEMENT

product vehicle (sunflower oil)

Limosilactobacillus reuteri CCT 7862

Limosilactobacillus reuteri CCT 7862 - 1 x 10e9 UFC/ daY.

Group Type EXPERIMENTAL

Limosilactobacillus reuteri CCT 7862

Intervention Type DIETARY_SUPPLEMENT

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.

Group Type EXPERIMENTAL

Bifidobacterium lactis CCT 7858 + Lactobacillus rhamnosus CCT 7863

Intervention Type DIETARY_SUPPLEMENT

Bifidobacterium lactis CCT 7858 + Lactobacillus rhamnosus CCT 7863 - 1 x 10e9 UFC/ day

Interventions

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Placebo

product vehicle (sunflower oil)

Intervention Type DIETARY_SUPPLEMENT

Limosilactobacillus reuteri CCT 7862

Limosilactobacillus reuteri CCT 7862 - 1 x 10e9 UFC/ day.

Intervention Type DIETARY_SUPPLEMENT

Bifidobacterium lactis CCT 7858 + Lactobacillus rhamnosus CCT 7863

Bifidobacterium lactis CCT 7858 + Lactobacillus rhamnosus CCT 7863 - 1 x 10e9 UFC/ day

Intervention Type DIETARY_SUPPLEMENT

Eligibility Criteria

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Inclusion Criteria

* Age 20 days ± 3 days.
* Informed consent form signed by parents
* Both gender
* Availability to complete scales daily and answer phone calls and/or text messages.

Exclusion Criteria

* Birth weight \<2500 g;
* 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.
Minimum Eligible Age

17 Days

Maximum Eligible Age

23 Days

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Universidade do Extremo Sul Catarinense - Unidade Academica de Ciecias da Saude

OTHER

Sponsor Role lead

Responsible Party

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Monique Michels

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Monique Michels

Criciúma, Santa Catarina, Brazil

Site Status RECRUITING

Countries

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Brazil

Facility Contacts

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monique michels, PhD

Role: primary

+5548996274651

Other Identifiers

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63543922.2.0000.0119

Identifier Type: -

Identifier Source: org_study_id

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