Effects of Vaginal Seeding on Infants' Body Mass Index and Allergy Risk for Caesarean-delivered Children
Overweight and Obesity, Allergy
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
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
Experimental
No Intervention
Vaginal seeding group
Control group
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