About this trial
The purpose of this study is to further investigate the association between vitamin D deficiency/insufficiency and hypertensive disorders of pregnancy by studying the impact of screening for vitamin D deficiency and supplementation when low levels of vitamin D are detected. Screening for vitamin D deficiency (less than 20 ng/mL) and insufficiency (less than 30 ng/mL) may determine the need for additional supplementation, as most prenatal vitamins only contain 400 IU of vitamin D. The rates of hypertensive disorders of pregnancy amongst patients who received supplementation and maintained adequate vitamin D levels will be followed.
Eligibility criteria
Qualifiers
Pregnant women
18-45 years old
Receiving care at outpatient OB office of TriHealth's Women's Services Comprehensive OB-GYN Team with a plan to deliver at Bethesda North Hospital
Disqualifiers
Non-English speaking
Unable to provide consent to research study participation
Diagnosis of preexisting renal disease
Diagnoses of preexisting chronic hypertension
Trial design
Treatments tested in this trial
- Vitamin D Levels measurement