Modulation of Bifidocentric Dysbiosis Through Bifidobacterium Bifidum PRL2010 Supplementation in Caesarian-born Infants

Sponsor
Liaquat University of Medical & Health Sciences (Other)
Overall Status
Completed
CT.gov ID
NCT05936541
Collaborator
Ospedale Santa Maria Goretti (Other)
20
1
2
16.6
1.2

Study Details

Study Description

Brief Summary

This study is aimed to manipulate the composition of the intestinal flora of the infants born by caesarian section through the administration of the probiotic strain "Bifidobacterium bifidum PRL 2010", in order to evaluate its effects on gut dysbiosis during the first 6 month of life.

Condition or Disease Intervention/Treatment Phase
  • Dietary Supplement: Probiotic Bifidobacterium Bifidum PRL2010
  • Other: Control group
N/A

Detailed Description

There has been increasing interest in the field of human microbiome, considering its impact on health and diseases. The gastrointestinal tract represents the most heavily inhabited organ with microorganisms, counting 10 times the total number of human cells; for this reason, the gut microbiome has recently been referred as a proper organ. Intestinal microbial composition is unique for each individual and it is influenced by numerous factors, of which delivery mode is an important one with gestational age of the newborn, type of feeding and intrapartum or neonatal antibiotic therapy. Recent reports suggest that dysbiosis secondary to delivery mode affects the subsequent regulation of immune response and may be associated with several pathologic conditions, for example allergic diseases or obesity. Moreover, gut microbiome seems to impact on neurodevelopment during first six months of life. Bifidobacteria is the most represented group of intestinal microbiota in the newborn, followed by Enterobacteria, and it plays an important role in the infant gut. This includes the fundamental function performed by Bifidobacterium bifidum: it supplies the nutritional material to the rest of the microbial community, particularly Bifidobacterium breve and Bifidobacterium longum infantis that are the other typical bifidobacteria of the newborn. It is a powerful metabolizer of the intestinal mucus and the HMOs (Human Milk Oligosaccharides) present in breast milk. Thanks to its exocitable enzymes, the degradative catabolism occurs in the intestinal environment. Thus, B. bifidum favour the increase in intestinal richness and biodiversity (9), which correlates with the host's state of health. However, bifidobacteria is reduced in infants born by cesarean delivery.

Aim of the study is to assess if the Bifidobacterium Bifidum PRL2010 supplementation effectively ameliorat bifidocentric dysbiosis due to the delivery mode and we want to confirm this by analyzing fecal microbiota in caesarean birth infants.

Study Design

Study Type:
Interventional
Actual Enrollment :
20 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Probiotic Bifidobacterium Bifidum PRL2010Probiotic Bifidobacterium Bifidum PRL2010
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Modulation of Bifidocentric Dysbiosis Through Bifidobacterium Bifidum PRL2010 Supplementation in Caesarian-born Infants
Actual Study Start Date :
Jan 5, 2020
Actual Primary Completion Date :
May 2, 2021
Actual Study Completion Date :
May 25, 2021

Arms and Interventions

Arm Intervention/Treatment
Experimental: Probiotic Bifidobacterium Bifidum PRL2010

Participants in this group will receive probiotic Bifidobacterium Bifidum PRL2010 supplementation from the time of discharge to a daily for the 6 months

Dietary Supplement: Probiotic Bifidobacterium Bifidum PRL2010
Probiotic supplement

Active Comparator: Control

Participants in this group will not receive probiotic probiotic supplementation

Other: Control group
No probiotic supplementation

Outcome Measures

Primary Outcome Measures

  1. Number of participants with disease [up to 6 months]

    Number of participants with skin, respiratory and gastrointestinal diseases assessed with a questionnaire submitted to parents

Secondary Outcome Measures

  1. Variation in children gut microbiota composition [up to 6 months]

    Variation in gut microbiota composition of children born by caesarean section assessed by faecal colonic microbiota analysis with 16S rRNA technology

Eligibility Criteria

Criteria

Ages Eligible for Study:
1 Month to 1 Year
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Healthy infants born by caesarian delivery

  • Parents informed written consent

Exclusion Criteria

  • Suspension of the administration of the probiotic strain for a period of time exceeding 7 days

  • Interruption of the administration of the probiotic strain before the completion of the sixth month

  • Replacement of Bifidobacterium bifidum PRL2010 with another strain

  • Refusal to collect the fecal sample expressed by parents

  • Major congenital birth deformities

  • Acute illness at enrollment

  • Any condition affecting food intake or metabolism

  • Maternal mental and psychosomatic diseases

Contacts and Locations

Locations

Site City State Country Postal Code
1 Neonatology and Neonatal Intensive Care Unit of Santa Maria Goretti Hospital Latina Italy LT 04100

Sponsors and Collaborators

  • Liaquat University of Medical & Health Sciences
  • Ospedale Santa Maria Goretti

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Dr. Amjad Khan, Professor of Clinical Biochemistry and Experimental Medicine, Liaquat University of Medical & Health Sciences
ClinicalTrials.gov Identifier:
NCT05936541
Other Study ID Numbers:
  • 04-10/05/2022
First Posted:
Jul 7, 2023
Last Update Posted:
Jul 7, 2023
Last Verified:
Jul 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 7, 2023