Cross sectional study to investigate the 25-hydroxyvitamin D level and potentially influencing factors of pregnant women and their newborns in Germany

• Conditions: E55.9; E55; Vitamin D deficiency, unspecified; Vitamin D deficiency

• Registration Number: DRKS00003245
• Lead Sponsor: Institut für Ernährungswissenschaft, JLU Giessen

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2011-09-07
• Study Completion: 2012-02-29
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 328

Inclusion Criteria

Pregnant women and their newborns, delivery at the St. Josefs Hospital Giessen

Exclusion Criteria

Hypercalcaemia, secondary hyperparathyroidism, granulomatosis, malabsorption diseases, history of chronic liver or kidney disease, intake of anticonvulsants or Glucocorticoids, outpatient delivery

Study & Design

• Study Type: observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Determining maternal and newborn serum 25-hydroxy-vitamin D at time of delivery using chemiluminescence immunoassay (CLIA)

Secondary Outcome Measures

Name	Time	Method
Maternal serum and cord blood:<br>parathyroid hormone, alkaline phosphatase and calcium at time of delivery