The purpose of this study is to determine whether fluoride supplementation during pregnancy is effective in extending the length of gestation and improving overall perinatal well-being.
The Centers for Disease Control and Prevention (CDC) reports that preterm birth affected about 1 in 10 infants born in the United States in 2015. These statistics emphasize the significance of implementing a safe and effective therapy into routine clinical care aimed at reducing the rate of preterm birth. There has been evidence to suggest that fluoride supplementation to women during pregnancy can provide other medical benefits, in addition to a reduction in dental caries. Fluoride is recognized by the Food and Nutrition Board (F\&NB) of the American Academy of Sciences and the Food \& Drug Administration (FDA) as an essential ion due to its association with a reduction in dental caries. Upon entering the body, fluoride is taken up into the bones/calcified tissues, and excreted by the kidneys. When supplied during pregnancy in small aliquots, as with water fluoridation, the fluoride is likely taken up in the mother's bones and excreted by her kidneys so rapidly, that the fetus is denied a meaningful amount of fluoride, unless it is supplied in a pulse dose by supplement. The Institute of Medicine's Food and Nutrition Board recommends 3 mg/day for Adequate Intake in pregnancy and deems 10 mg/day as the Upper Limit. After several papers elucidating an association between poor dentition, periodontal disease, and preterm birth, subsequent RCT's of regular periodontal scaling and treatment during pregnancy are still inconclusive in regards to preterm birth. The investigators hypothesize that fluoride supplementation during pregnancy may have a beneficial effect on the natural microbiome of the maternal oral cavity and genital tract, capable of protecting against transient bacteremia and ascending infection, respectively, which are known antecedents to both preterm labor and preterm premature rupture of membranes. The research team predicts that the testing and analysis of specimens collected will demonstrate microbiome changes toward a more favorable profile not associated with preterm birth. The proposed randomized, double-blinded, placebo-controlled clinical trial aims to confirm the efficacy of fluoride supplementation in pregnancy to extend length of gestation and increase overall perinatal well-being, and to confirm transplacental transfer of supplemental fluoride. This research may also identify other beneficial maternal and neonatal outcomes associated with the administration of fluoride during the perinatal period by attempting to characterize and compare the microbiomes of the maternal oral cavity and genital tracts between supplemented and unsupplemented gravidas.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
OTHER
Masking
QUADRUPLE
Enrollment
43
Prenatal vitamin-mineral containing 3 mg fluoride to be taken daily, starting at 10-20 weeks gestation until delivery.
Prenatal vitamin-mineral containing 0 mg fluoride to be taken daily, starting at 10-20 weeks gestation until delivery.
Johns Hopkins Hospital
Baltimore, Maryland, United States
Length of gestation
the length of gestation will be measured in weeks at time of delivery
Time frame: Participants will be followed from the time of study enrollment until delivery, up to 30 weeks total in the study
Birth weight
Birth weight will be measured in grams and pounds
Time frame: Participants will be followed from the time of study enrollment until delivery, up to 30 weeks total in the study
Birth length
birth length will be measured in inches
Time frame: Participants will be followed from the time of study enrollment until delivery, up to 30 weeks total in the study
Preterm birth
Preterm birth will be measured in weeks at time of delivery
Time frame: Participants will be followed from the time of study enrollment until delivery, up to 30 weeks total in the study
Preterm premature rupture of membranes (PPROM)
PPROM will be measured in weeks at time of PPROM
Time frame: Participants will be followed from the time of study enrollment until delivery, up to 30 weeks total in the study
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