Prevalence of Vitamin D Deficiency in Pregnant Women and Their Fetus in North Jordan
NCT ID: NCT04944212
Last Updated: 2023-03-10
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
396 participants
OBSERVATIONAL
2021-10-31
2022-07-30
Brief Summary
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1. Determine vitamin D levels among newborns born in north Jordan
2. Determine vitamin D levels among pregnant women in north Jordan
3. Study the association between maternal and infants levels of vitamin D
4. Explore the association between maternal and fetal characteristics and maternal and/or fetal vitamin D level
5. Study the effect of low fetal vitamin D on newborn anthropometry
6. Study the effect of maternal vitamin D supplement use during pregnancy in raising cord serum vitamin D levels
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Detailed Description
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5 ml of venous blood will be obtained from pregnant women at the time of admission and 3 ml of venous blood will be obtained from the umbilical cord veins of the newborns immediately after their delivery. The quantitative measurement of 25OHD in serum will be performed using ELIZA.
Investigators will determine the means, medians and standard deviations of 25OHD levels among pregnant women and infants in Jordan. In addition, investigators will study the association between maternal and infants levels of 25OHD. Moreover, investigators will investigate the association between maternal level of vitamin D and elective maternal variables including vitamin D supplements during and before pregnancy, sun exposure, age, weight, parity, BMI, \& maternal medical problems. In addition, investigators will study the effect of low fetal vitamin D on newborn anthropometry. Finally, investigators will study the effect of maternal vitamin D supplements use during pregnancy in raising cord serum vitamin D levels
Conditions
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Study Design
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OTHER
CROSS_SECTIONAL
Interventions
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Measuring vitamin D serum level using ELIZA
Venous blood will be obtained from pregnant women at the time of admission and from the umbilical cord veins of the newborns immediately after their delivery. The quantitative measurement of 25OHD in serum will be performed using ELIZA.
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
ALL
No
Sponsors
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Jordan University of Science and Technology
OTHER
Responsible Party
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Principal Investigators
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Rawan A Obeidat, Dr
Role: PRINCIPAL_INVESTIGATOR
Jordan University of Science and Technology
Locations
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King Abdullah University Hospital
Irbid, , Jordan
Countries
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Other Identifiers
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39/131/2020
Identifier Type: -
Identifier Source: org_study_id
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