Vitamin D and Hypertensive Disorders of Pregnancy

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-45
SponsorTriHealth Inc.

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

Treatment groups

594 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators