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Clinical Trials/NCT02567071
NCT02567071CompletedNot Applicable

Retablissement Du Microbiote Naturel Apres Naissance Par Cesarienne

Institut National de la Santé Et de la Recherche Médicale, France2 sites in 1 country33 target enrollmentStarted: April 6, 2016Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
33
Locations
2
Primary Endpoint
Diversity of the intestinal microbiota

Study Overview

Brief Summary

The proportion of cesarean deliveries reached 30% of births in the US in 2008, while in the 1970s, it rarely reached 15%, as recommended by WHO. According to recent reports in some hospitals in China the use of cesarean section increased from 5% in the 1970s to over 60%. The use of C-section continues to grow in every countries of the world despite that current knowledge leads us to think that the vaginal birth, retained through millennia during mammalian evolution, guarantees the implementation of the best suited intestinal microbiota to build immunity and beneficial protective functions under the balanced mutual association between the host and its microbiota. Oral administration of a previously impregnated swab, by vaginal and maternal perineal secretions, following birth by planned C-section, would restore the normal development of the newborn intestinal microbiota mimicking exposure to these secretions during vaginal delivery.

The expected benefit is the establishment of a rich and diverse microbiota in individuals in the intervention group and by extension improving the overall health of these individuals.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Other
Masking
Single (Participant)

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
Female
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • over the age of legal majority
  • delivery by planned C-section at term or vaginal delivery at term
  • registered at a social security service

Exclusion Criteria

  • HIV or other STD patients
  • immunocompromised patients
  • known streptococcus B carriers
  • known vaginal or perineal herpes infections
  • chronic disease patients (obesity, diabetes, IBD)
  • IMC before pregnancy > 30 kg/m²
  • antibiotic treatments one month before delivery
  • emergency C-section
  • Premature delivery (<37 amenorrhea weeks)
  • hospitalized for more than one week before delivery
  • known HVC infections
  • for the newborns: every diagnosed anomaly
  • patients who do not understand the research procedures or those that are institutionalized, or those unable to give informed consent
  • patients deprived of ther liberty by legal or administrative decisions
  • patients under an exclusion period from another study

Arms & Interventions

Placebo Group

Placebo Comparator

75 children born by planned C-section will be exposed to clean swab.

Intervention: clean swab (Other)

Control Group

No Intervention

75 children born vaginally.

Intervention Group

Experimental

75 children born by planned C-section will be exposed to the perineal microbiota of their mothers through perineal impregnated swab.

Intervention: perineal impregnated swab (Other)

Outcomes

Primary Outcomes

Diversity of the intestinal microbiota

Time Frame: 1 year

Intestinal microbiota diversity will be evluated through metagenomics.

Secondary Outcomes

  • Health status(1 year)

Investigators

Sponsor
Institut National de la Santé Et de la Recherche Médicale, France
Sponsor Class
Other Gov
Responsible Party
Sponsor

Study Sites (2)

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