Vitamin D Deficiency Clinical Trial
— GRAVITDOfficial title:
Vitamin D Deficiency in Pregnancy - Identifying Associations and Mechanisms Linking Maternal Vitamin D Deficiency to Placental Dysfunction and Adverse Pregnancy Outcomes
NCT number | NCT04291313 |
Other study ID # | GRAVITD |
Secondary ID | |
Status | Recruiting |
Phase | N/A |
First received | |
Last updated | |
Start date | June 8, 2020 |
Est. completion date | May 2023 |
Danish pregnant women are recommended ad daily vitamin D supplement of 10 µg. Despite the fact that 9 out of 10 women take vitamin D supplements, more than 40% of pregnant women are vitamin D deficient, putting them at an increased risk of pregnancy complications like fetal growth restriction and pre-eclampsia. Our hypothesis is that pregnant women would benefit from an increased intake og vitamin D and that an intake of 90µg/day can reduce the prevalence of placenta-related pregnancy complications. Combining a double-blinded randomized trial (10µg vs.90µg) with collection of placental material, we want to test if the prevalence of pregnancy complications is reduced and explore how vitamin D affects placenta to improve our understanding of the disease pathology and risk factors.
Status | Recruiting |
Enrollment | 2000 |
Est. completion date | May 2023 |
Est. primary completion date | February 2023 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - All pregnant women attending the nuchal translucency scan in week 11-13 of gestation as part of the national prenatal screening program Exclusion Criteria: - Age< 18 years - Women with calcium metabolism disorders, - Women who gets doctor prescribed vitamin D treatment - Women with chronic kidney disease |
Country | Name | City | State |
---|---|---|---|
Denmark | Department of Biomedicine, University of Aarhus | Aarhus | |
Denmark | Randers Regional Hospital | Randers |
Lead Sponsor | Collaborator |
---|---|
University of Aarhus |
Denmark,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | The prevalence of pre-eclampsia (PE) | The effect of 90 µg on the prevalence of PE | From 20 weeks of gestation to delivery | |
Primary | The prevalence of fetal growth retardation (FGR) | The effect of 90 µg on the prevalence of FGR | From 20 weeks of gestation to delivery | |
Primary | The prevalence of gestational diabetes (GDM) | The effect of 90 µg on the prevalence of GDM | From 20 weeks of gestation to delivery | |
Secondary | Changes in the placental expression of genes- and proteins related to vitamin D, evaluated using Next Generation Sequencing (NGS), quantitative Polymerase Chain Reaction (qPCR), methylation (Bisulfite conversion) and western blotting. | Characterization of the changes in the placenta as a result of vitamin D deficiency in healthy women including evaluation of the effect of BMI on placental function and vitamin D metabolism.
NGS will be used to obtain a pathway analysis of differences between groups. Important findings from NGS will be verified on genetic and protein levels by qPCR and Western blotting respectively. Findings from NGS, qPCR and western blotting will be combined to characterize the changes in placentas from vitamin D deficient women compared to vitamin D sufficient women stratified by BMI. Further, changes in the expression of pivotal genes/proteins related to vitamin D metabolism (CYP2R1, CYP27B1, CYP24A1, Vitamin D receptor) will be investigated using qPCR, methylation analysis and western blotting. Findings from qPCR (gene level) methylation (gene level) and western blotting (protein level) are combined to characterize changes in placentas. Analyses will be done in subgroups of participants |
At delivery | |
Secondary | Changes in the placental expression of genes- and proteins related to vitamin D and the pathogenesis of PE, FGR and GDM in placental tissue from complicated pregnancies compared to uncomplicated pregnancies, evaluated using NGS, qPCR and western blotting | Identification of changes in placental expression of genes and proteins related to the pathogenesis of PE, FGR and GDM and their relationship to vitamin D sensitive placental functions in complicated pregnancies (PE, FGR, GDM) compared to healthy uncomplicated pregnancies.
NGS will be used to obtain a pathway analysis of differences in the gene expression between complicated pregnancies (PE, FGR, GDM) and healthy uncomplicated pregnancies. Important findings from the NGS studies will be verified on genetic and protein levels by qPCR and Western blotting. Findings from the NGS and the verifying results from qPCR (gene level) and western blotting (protein level) will be combined to characterize the changes in placentas from complicated pregnancies (PE, FGR, GDM) compared to healthy uncomplicated pregnancies. Analyses will be done in subgroups of participants |
At delivery | |
Secondary | Birthweight | The effect of 90 µg vitamin D on birthweight. | At delivery | |
Secondary | Size related to gestational age | The effect of 90 µg vitamin D on size related to gestational age (Small for Gestational Age;SGA, Appropriate for Gestational Age; AGA, Large for Gestational Age;LGA) | At delivery | |
Secondary | The prevalence of preterm birth | The effect of 90 µg vitamin D on the prevalence of preterm birth (birth < 37 weeks of gestation). | At delivery | |
Secondary | The prevalence of postterm birth | The effect of 90 µg vitamin D on the prevalence of postterm birth (birth > 40 weeks of gestation) | At delivery | |
Secondary | The prevalence of gestational hypertension | The effect of 90 µg vitamin D on the prevalence of gestational hypertension (>140/90) | From 20 weeks of gestation to delivery | |
Secondary | Mode of delivery | Mode of delivery | At delivery | |
Secondary | The prevalence of infection during delivery | Infection during delivery (incl. use of antibiotics) | At delivery | |
Secondary | Admission to the neonatal ward | Admission of the new born child to the neonatal ward | The first two weeks after birth | |
Secondary | Prevalence of post partum hemorrhage > 500 ml | The effect of 90 µg vitamin D on the prevalence of post partum hemorrhage > 500 ml | The first 24 hours after delivery |
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