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Probiotics, Respiratory and Intestinal Microbiome and Respiratory Tract Infections in Children

Primary Purpose

Respiratory Infections in Children

Status
Unknown status
Phase
Phase 1
Locations
Mexico
Study Type
Interventional
Intervention
Bacillus clausii
Sterile water
Sponsored by
Universidad Nacional Autonoma de Mexico
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Respiratory Infections in Children focused on measuring Respiratory infections, Probiotics, Microbiome, Viruses, Children

Eligibility Criteria

3 Hours - 2 Days (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Heathy term newborns
  • Vaginal or cesarean section delivery
  • Informed consent of both parents to participate

Exclusion Criteria:

  • Preterm newborns
  • Co-morbidities

Sites / Locations

  • Rosa Maria Wong-ChewRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Probiotics

Placebo group

Arm Description

Probiotics consist on Bacillus clausii in a plastic vial that will be administered to the infant 4 times a week

Sterile water contained in a plastic vial will be administered to the infant 4 times a week

Outcomes

Primary Outcome Measures

Number of respiratory infections in the first year of life
Follow up of the infants will be performed every 2 months during 1 year to look at the incidence of respiratory tract infections in each arm

Secondary Outcome Measures

Rates of bacterial phyla in nasal and intestinal washes
Nasal washes and stool samples will be taken and analyzed for the microbiome. The proportion of phyla will be compared between the probiotic and placebo groups.
Number of viruses detected in nasal washes during the follow up
Nasal washes will be taken every 2 months during 1 year to detect by multiplex polymerase chain reaction viruses that could be in the nasopharynx of the children

Full Information

First Posted
September 21, 2018
Last Updated
September 25, 2018
Sponsor
Universidad Nacional Autonoma de Mexico
Collaborators
Hospital General de Mexico
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1. Study Identification

Unique Protocol Identification Number
NCT03683927
Brief Title
Probiotics, Respiratory and Intestinal Microbiome and Respiratory Tract Infections in Children
Official Title
The Impact of Probiotics in the Respiratory and Gastrointestinal Microbiome and Its Role in Respiratory Tract Infections in Children
Study Type
Interventional

2. Study Status

Record Verification Date
September 2018
Overall Recruitment Status
Unknown status
Study Start Date
January 10, 2018 (Actual)
Primary Completion Date
January 9, 2020 (Anticipated)
Study Completion Date
March 10, 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Universidad Nacional Autonoma de Mexico
Collaborators
Hospital General de Mexico

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Pneumonia and diarrhea are the most frequent causes of infectious diseases in children under 5 years of age worldwide, responsible for 1.5 million deaths annually. In up to 80% of pneumonia cases the etiology is viral. Some viruses can persist up to 6 months after an acute infection. The time when viruses enter the body and whether they are commensals or only cause disease and are eliminated after an acute infection is unknown. Modern techniques have identified diverse communities of microbiota in healthy and sick people, and viral communities associated in a close interaction. The acquisition and colonization by respiratory viruses and the role in health and disease in this niche that is the microbiome is unknown. The role of probiotics in the prevention of respiratory disease and in the maintenance of homeostasis in the microbiota is poorly understood, and even more the probable relationship between the microbiota, the respiratory viruses that could be commensals or pathogens at the respiratory level, the time when children can be colonized, and their regulation with the administration of probiotics. The aims of the study are to determine the changes in the intestinal and respiratory microbiota, the viruses that can be commensals or cause disease and the role of probiotics in the prevention of respiratory diseases during the first year of life. A prospective, randomized, controlled clinical trial will be carried out making basic metagenomics studies (translational medicine). After informed consent, 120 newborns will be randomized into 2 groups, one will receive probiotics 4 times a week orally and the other a placebo consisting of sterile water 4 times a week. The clinical follow up will be done every 2 months until 1 year old, nasal washes and stool samples will be collected to determine the intestinal and respiratory microbiome. Multiplex polymerase chain reaction studies will be conducted to detect the presence of respiratory viruses and the time when the children acquire viruses that are commensal or only in the case of respiratory infection. The mothers will be asked to come for consult in case of respiratory infection and a nasal wash and stool sample will be taken. Descriptive, bivariate and multivariate statistics will be used to determine the associations between the microbiota, the viral metagenomics, the respiratory viruses and the risk of presenting or not respiratory infection in the group receiving probiotics compared to placebo.
Detailed Description
Pneumonia and diarrhea are the 2 most frequent causes of infectious diseases in children under 5 years of age worldwide, responsible for 1.5 million deaths annually. In 2013, they corresponded to 15% and 9%, respectively, of the 6.3 million deaths in children under 5 years of age. In our country according to the Ministry of Health, acute respiratory infections are the leading cause of disease nationwide with 27,493, 239 cases reported in 2014 in which pneumonia ranks 19th in the top 20 causes of disease with 174,748 cases, of which 51,893 cases (29%) are in children under 5 years of age, and 21,404 cases (12%) in children under 1 year old; in 2015, 148,140 cases of pneumonia were reported. It is estimated that in up to 80% of pneumonia cases the etiology is viral. It has been reported that some viruses such as adenovirus or bocavirus can persist up to 6 months after an acute infection. The time when viruses enter the body and whether they are commensals of the respiratory tract or only cause disease and are eliminated after an acute infection is unknown. Modern techniques have identified diverse communities of microbiota in healthy and sick people, and viral communities associated in a close interaction, which has changed concepts of pathogenesis of respiratory tract infections. The interaction of respiratory viruses, the acquisition and colonization by respiratory viruses and the role in health and disease in this niche that is the microbiome is not known. The role of probiotics in the prevention of respiratory disease and in the maintenance of homeostasis in the microbiota is poorly studied, and even more the probable relationship between the microbiota, the viroma, the respiratory viruses that could be commensals or pathogens at the respiratory level, the time when children can be colonized, and their regulation with the administration of probiotics. The aims of the study are to determine the changes in the intestinal and respiratory microbiota, the intestinal and respiratory viroma, the viruses that can be commensals or cause disease and the role of probiotics in the prevention of respiratory diseases during the first year of life. Methods A prospective, randomized, controlled clinical trial will be carried out making basic metagenomics studies applied to the clinic (translational medicine). In this study the investigators plan to follow up a cohort of 120 children from newborns to one year of age. After informed consent, children will be randomized into 2 groups, one will receive probiotics 4 times a week orally and the other a placebo consisting of sterile water 4 times a week. The clinical follow up will be done every 2 months, where nasal washes and stool samples will be collected to determine the intestinal and respiratory microbiome and the viral metagenomics. Multiplex polymerase chain reaction studies will be conducted to detect the presence of respiratory viruses and detect the time when the children acquire viruses that are commensal or only in case of respiratory infection with manifestations of disease. The mothers will document and will be asked to come for consult in case of respiratory infection, in which samples of nasal washes will be taken to determine the virus or bacteria that could be causing the infection. Descriptive, bivariate and multivariate statistics will be used to determine the associations between the microbiota, the viral metagenomics, the respiratory viruses and the risk of presenting or not respiratory infection in the group receiving probiotics compared to placebo. A p< 0.05 will be considered statistically significant.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Respiratory Infections in Children
Keywords
Respiratory infections, Probiotics, Microbiome, Viruses, Children

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
120 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Probiotics
Arm Type
Experimental
Arm Description
Probiotics consist on Bacillus clausii in a plastic vial that will be administered to the infant 4 times a week
Arm Title
Placebo group
Arm Type
Placebo Comparator
Arm Description
Sterile water contained in a plastic vial will be administered to the infant 4 times a week
Intervention Type
Combination Product
Intervention Name(s)
Bacillus clausii
Intervention Description
The probiotic (Bacillus clausii) will be administered 4 times a week to the infant
Intervention Type
Other
Intervention Name(s)
Sterile water
Intervention Description
The placebo group will receive sterile water 4 times a week
Primary Outcome Measure Information:
Title
Number of respiratory infections in the first year of life
Description
Follow up of the infants will be performed every 2 months during 1 year to look at the incidence of respiratory tract infections in each arm
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Rates of bacterial phyla in nasal and intestinal washes
Description
Nasal washes and stool samples will be taken and analyzed for the microbiome. The proportion of phyla will be compared between the probiotic and placebo groups.
Time Frame
1 year
Title
Number of viruses detected in nasal washes during the follow up
Description
Nasal washes will be taken every 2 months during 1 year to detect by multiplex polymerase chain reaction viruses that could be in the nasopharynx of the children
Time Frame
1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
3 Hours
Maximum Age & Unit of Time
2 Days
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Heathy term newborns Vaginal or cesarean section delivery Informed consent of both parents to participate Exclusion Criteria: Preterm newborns Co-morbidities
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Rosa M Wong-Chew, MD, DSc
Phone
5255 56232300
Ext
43193
Email
rmwong@unam.mx
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rosa M Wong-Chew, MD, DSc
Organizational Affiliation
Facultad de Medicina, Universidad Nacional Autonoma de Mexico
Official's Role
Principal Investigator
Facility Information:
Facility Name
Rosa Maria Wong-Chew
City
Mexico city
ZIP/Postal Code
04510
Country
Mexico
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Rosa M Wong-Chew, MD
Phone
5556232300
Email
rmwong@unam.mx
First Name & Middle Initial & Last Name & Degree
Bogart Espinosa Torres Torija, MD
First Name & Middle Initial & Last Name & Degree
Brenda Hernandez Perez, MD

12. IPD Sharing Statement

Plan to Share IPD
No

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Probiotics, Respiratory and Intestinal Microbiome and Respiratory Tract Infections in Children

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