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Effects of Vaginal Seeding on Infants' Body Mass Index and Allergy Risk for Caesarean-delivered Children

Primary Purpose

Overweight and Obesity, Allergy

Status
Active
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Vaginal seeding
Sponsored by
Peking University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Overweight and Obesity focused on measuring Body mass index, Allergic risk, Vaginal seeding, Randomized controlled study, Caesarean delivery, Overweight and obesity

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • local resident in Liuyang city
  • Singleton, term pregnancy (≥37 weeks of gestation)
  • Cesarean section before labor starts without maternal complications, or cesarean section after the start of labor but the cervix is less than 3 cm
  • Vaginal pH< 4.5 at enrollment

Exclusion Criteria:

  • Positive testing for HIV, HBV, syphilis or GBS infection at gestation
  • Vaginal infections such as genital herpetic lesions or chlamydia
  • Bacterial vaginosis
  • Trichomonas or fungous in leucorrhea
  • Pregnant women or her spouse with severe allergic diseases, such as asthma and severe drug allergy
  • Vaginal pH ≥4.5 at 1-2 hours before the cesarean section
  • Other conditions not suitable for intervention as judged by obstetricians

Sites / Locations

  • Liuyang Maternal and Child Health Care Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Vaginal seeding group

Control group

Arm Description

Swabbing infants born by C-section with a gauze incubated in the maternal vagina about an hour before the C-section. The gauze will be extracted prior to the C-section, kept in a sterile container in an incubator (37 ℃), and taken out from the incubator immediately before the swabbing. The infant will be swabbed with the gauze, starting from the lips, followed by the face, thorax, arms, legs, genitals and anal region, and finally the back. The swabbing will take around 15-20 seconds.

Managed based on the standard practice in the study site

Outcomes

Primary Outcome Measures

infant's body mass index
Body mass index in original scale and z-score
infant's body mass index
Body mass index in original scale and z-score
infant's body mass index
Body mass index in original scale and z-score
infant's body mass index
Body mass index in original scale and z-score
infant's allergy risk score
Calculated based on the measurements of multiallergens with 0-6 classes,higher values represent a worse outcome which means more susceptible to allergic diseases

Secondary Outcome Measures

Infants' gut microbiota profile
Intestinal flora will be detected by 16sRNA sequencing using feces samples
Rate of overweight/obesity
Defined by body mass index
Rate of allergic symptoms and common allergic diseases
Collected by using a structured questionnaire
Rate of adverse effects
Infection-related diseases and others

Full Information

First Posted
November 17, 2018
Last Updated
December 9, 2021
Sponsor
Peking University
Collaborators
National Natural Science Foundation of China, Liuyang Maternal and Child Health Care Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03809390
Brief Title
Effects of Vaginal Seeding on Infants' Body Mass Index and Allergy Risk for Caesarean-delivered Children
Official Title
Effects of Vaginal Seeding on Infants' Body Mass Index and Allergy Risk for Caesarean-delivered Children: A Randomized Controlled Study
Study Type
Interventional

2. Study Status

Record Verification Date
December 2021
Overall Recruitment Status
Active, not recruiting
Study Start Date
November 17, 2018 (Actual)
Primary Completion Date
September 20, 2021 (Actual)
Study Completion Date
November 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Peking University
Collaborators
National Natural Science Foundation of China, Liuyang Maternal and Child Health Care Hospital

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
This is a single-blind randomized controlled trial, aiming to evaluate the effects of vaginal seeding on body mass index as well as allergy risk for cesarean-delivered infants. It will be conducted in Liuyang city of China, and the targeted sample size is 106. All the eligible pregnant women will be randomly assigned to either the intervention or control group, and their babies of the participants will be followed up to 24 months of age.
Detailed Description
Many studies have suggested that caesarean-delivered children are at higher risks of developing metabolic and allergic diseases like obesity and asthma, possibly because newborns born by caesarean section were lack of exposure to maternal vaginal flora. It is needed to explore a simple, convenient, and safe intervention strategy to reduce caesarean-related risks. In a recent non-randomized study, the authors found that exposure of caesarean-delivered newborns to maternal vaginal fluid at birth (i.e., vaginal seeding) could partially restore the microbiota of them at 30 days after births, but the long-term health consequences of restoring the microbiota of caesarean-delivered infants remain unclear. In this randomized study, the investigators aim to examine whether the changes in newborns' microbiota will persist to 24 month of age, and whether vaginal seeding will have any effects on body mass index and allergy risk from birth to 24 months of age. the investigators will enroll a total of 106 pregnant women, and the participants' infants will be followed up at 0 (before hospital discharge), 6, 12, 18 and 24 months. At each follow-up visit, a questionnaire survey including information on feeding, medication, and allergic status will be conducted, infants' height and weight will be measured, and feces will be collected. At 18-month-old visit, infants' venous blood will be also collected for the assay of multiallergen. The primary outcomes were body mass index and allergy risk index. The secondary outcomes included the microbiota profile, allergic symptoms and diseases, overweight/obesity, and adverse effects.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Overweight and Obesity, Allergy
Keywords
Body mass index, Allergic risk, Vaginal seeding, Randomized controlled study, Caesarean delivery, Overweight and obesity

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
117 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Vaginal seeding group
Arm Type
Experimental
Arm Description
Swabbing infants born by C-section with a gauze incubated in the maternal vagina about an hour before the C-section. The gauze will be extracted prior to the C-section, kept in a sterile container in an incubator (37 ℃), and taken out from the incubator immediately before the swabbing. The infant will be swabbed with the gauze, starting from the lips, followed by the face, thorax, arms, legs, genitals and anal region, and finally the back. The swabbing will take around 15-20 seconds.
Arm Title
Control group
Arm Type
No Intervention
Arm Description
Managed based on the standard practice in the study site
Intervention Type
Procedure
Intervention Name(s)
Vaginal seeding
Intervention Description
The same as that stated in arm descriptions.
Primary Outcome Measure Information:
Title
infant's body mass index
Description
Body mass index in original scale and z-score
Time Frame
At 6 months
Title
infant's body mass index
Description
Body mass index in original scale and z-score
Time Frame
At 12 months
Title
infant's body mass index
Description
Body mass index in original scale and z-score
Time Frame
At 18 months
Title
infant's body mass index
Description
Body mass index in original scale and z-score
Time Frame
At 24 months
Title
infant's allergy risk score
Description
Calculated based on the measurements of multiallergens with 0-6 classes,higher values represent a worse outcome which means more susceptible to allergic diseases
Time Frame
At 18 months after birth
Secondary Outcome Measure Information:
Title
Infants' gut microbiota profile
Description
Intestinal flora will be detected by 16sRNA sequencing using feces samples
Time Frame
At baseline (Meconium), 6, 12 ,18 and 24 months after birth
Title
Rate of overweight/obesity
Description
Defined by body mass index
Time Frame
At 6, 12 ,18 and 24months
Title
Rate of allergic symptoms and common allergic diseases
Description
Collected by using a structured questionnaire
Time Frame
At 61, 12 ,18 and 24 months
Title
Rate of adverse effects
Description
Infection-related diseases and others
Time Frame
From birth to 24 months

10. Eligibility

Sex
Female
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: local resident in Liuyang city Singleton, term pregnancy (≥37 weeks of gestation) Cesarean section before labor starts without maternal complications, or cesarean section after the start of labor but the cervix is less than 3 cm Vaginal pH< 4.5 at enrollment Exclusion Criteria: Positive testing for HIV, HBV, syphilis or GBS infection at gestation Vaginal infections such as genital herpetic lesions or chlamydia Bacterial vaginosis Trichomonas or fungous in leucorrhea Pregnant women or her spouse with severe allergic diseases, such as asthma and severe drug allergy Vaginal pH ≥4.5 at 1-2 hours before the cesarean section Other conditions not suitable for intervention as judged by obstetricians
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jian-meng Liu, PhD
Organizational Affiliation
Peking University
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Hong-tian Li, PhD
Organizational Affiliation
Peking University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Shujin Zhou, MD
Organizational Affiliation
Liuyang Maternal and Child Health Care Hospital
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Yang Liu, PhD Candidate
Organizational Affiliation
Peking University
Official's Role
Study Director
Facility Information:
Facility Name
Liuyang Maternal and Child Health Care Hospital
City
Liuyang
State/Province
Hunan
ZIP/Postal Code
410399
Country
China

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
The IPD will be shared upon the request of other researchers, and all the key variables that will be reported in the main paper are planned to be shared
IPD Sharing Time Frame
After the publication of the main paper (hopefully before the end of 2022), the data will be available to share to other researchers
IPD Sharing Access Criteria
Researchers should request the data via the following Email: lihongtian@pku.edu.cn or liujm@pku.edu.cn

Learn more about this trial

Effects of Vaginal Seeding on Infants' Body Mass Index and Allergy Risk for Caesarean-delivered Children

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